Valeska Schroeder, Ph.D. CEO & Chairman, Cerapedics Inc. Two FDA PMA-Approved Spinal Biologics Materials Scientist | Venture Investor | Operator UC Berkeley Ph.D. 150,000+ Patients Treated Worldwide Westminster, Colorado PearlMatrix: First Proven Bone Growth Accelerator for Lumbar Fusion Valeska Schroeder, Ph.D. CEO & Chairman, Cerapedics Inc. Two FDA PMA-Approved Spinal Biologics Materials Scientist | Venture Investor | Operator UC Berkeley Ph.D. 150,000+ Patients Treated Worldwide Westminster, Colorado PearlMatrix: First Proven Bone Growth Accelerator for Lumbar Fusion
YesPress Profile — Medtech Executive

Valeska
Schroeder

Ph.D.  |  CEO & Chairman  |  Cerapedics Inc.

She studied atoms at Berkeley. Then she funded companies. Now she runs one that's changing how surgeons fuse the human spine.

Medtech CEO Materials Science Ph.D. FDA PMA x2 Venture Operator Spine Biologics
Valeska Schroeder, CEO of Cerapedics
Valeska Schroeder — Cerapedics Inc.
2 FDA PMA Approvals
150K+ Patients Treated
$162M Total Funding
3x UC Berkeley Degrees
The Story

The Scientist Who Wouldn't Stay in the Lab

In 2025, Cerapedics became the only company on earth holding two FDA PMA-approved bone grafts for spinal fusion. The person who made that happen started her career measuring the behavior of materials at the atomic scale. That's not a coincidence.

Valeska Schroeder earned her BS, MS, and PhD in Materials Science and Engineering from UC Berkeley - three degrees, one discipline, one university. That level of focus is either stubbornness or precision. In her case, it turned out to be the foundation for a career that has moved from the laboratory bench to the boardroom with unusual coherence.

After completing her doctorate, she worked in product development, program management, and marketing across multiple medical device companies - the kind of cross-functional exposure that most engineers spend careers avoiding. She was learning how things break, how they get approved, how they get sold, and crucially, how the gap between a promising technology and a patient outcome actually gets closed.

In 2016, she joined KCK MedTech as part of the firm's Medical Technologies Investment Group, eventually becoming Managing Director. KCK runs as a single-family evergreen fund - patient capital, long horizon. It's the kind of investor that backs technologies measured in decades, not quarters. The P-15 peptide at the core of Cerapedics' products had been in development for over 30 years when Schroeder first encountered it. She recognized what it was.

When KCK invested in Cerapedics in 2018, Schroeder joined the board. She was one of a handful of investors also serving on boards at Sight Sciences, Aerin Medical, Intuity Medical, and Lungpacer simultaneously - companies across ophthalmology, ENT, diabetes management, and pulmonary medicine. The thread connecting all of them: drug-device products tackling stubborn clinical problems with evidence-based technology.

By 2021, she had deepened her operational involvement with Cerapedics and taken the Chairman seat. A year later, on November 1, 2022, she became CEO. Greg Garfield, Senior Managing Director at KCK, described her as having demonstrated "leadership ability, clear vision for strategic growth and operational efficiency" during her board tenure. That's the kind of endorsement that turns investors into operators.

The years since have moved fast. Under her leadership, Cerapedics pushed PearlMatrix P-15 Peptide Enhanced Bone Graft through its pivotal ASPIRE study - a multi-center clinical trial for single-level lumbar fusion that showed statistically superior clinical success and, critically, more than twice as many patients achieving fusion at six months compared to local autograft. In June 2025, the FDA granted premarket approval. Cerapedics became the only company with two PMA-approved spinal biologics on the U.S. market - i-FACTOR for cervical fusion, PearlMatrix for lumbar. Two of only three such products in the country.

By January 2026, the FDA had approved expanded indications for PearlMatrix to cover not just transforaminal lumbar interbody fusion (TLIF) but also ALIF, PLIF, OLIF, and LLIF - essentially, every major lumbar approach a surgeon might take. That same year, a Vizient supplier agreement put Cerapedics products in reach of over 65% of U.S. acute care providers, including 97% of academic medical centers.

Schroeder lives in Menlo Park, California - the geographic heart of venture capital - but runs a company headquartered in Westminster, Colorado that's expanding its office space to accommodate growth. She's spoken publicly about supporting women leaders in medtech, and colleagues note she spends time in the outdoors when she's not in front of a screen. For a person who built her professional life on the science of how materials bind together, heal, and hold - that instinct toward the physical world makes a certain kind of sense.

The P-15 peptide she's staked Cerapedics' future on is a 15-amino-acid synthetic sequence that mimics a collagen binding domain. It doesn't grow bone itself. It activates the body's own osteogenic cells to do the work. Schroeder's career trajectory follows a similar logic: she doesn't replace the underlying systems, she activates them. Companies. Technologies. Teams. She finds the binding site and gets things moving.

"I am excited to lead Cerapedics as we advance through the next phase of the company. We look forward to delivering improved bone repair outcomes for patients, doctors, and payers with our innovative P-15 peptide technology."
- Valeska Schroeder, on becoming CEO, Nov. 2022
🏭
Company Snapshot
Cerapedics Inc.
Westminster, Colorado
~230 Employees
$162M Total Funding
$67M Annual Revenue
Est. company
🌞
The P-15 Peptide
A synthetic 15-amino-acid sequence mimicking collagen's binding domain. Activates the body's own osteogenic cells - it doesn't grow bone, it tells your cells to.
Science

From Lab Bench to Boardroom

Pre-2016
Medical Device Operator
Senior roles across product development, program management, and marketing at multiple medtech companies. Building fluency across the full commercial arc of regulated devices.
2016
Joins KCK MedTech as Investor
Enters single-family evergreen fund focused on medical technologies. Leads investments and advises portfolio companies across the medtech landscape. Becomes Managing Director.
2018
Joins Cerapedics Board
KCK invests in Cerapedics. Schroeder takes a board seat alongside other portfolio company boards at Sight Sciences, Aerin Medical, Intuity Medical, and Lungpacer.
2021
Becomes Chairman of the Board
Deepens operational involvement with Cerapedics. Takes the Chairman seat as the company prepares to scale its commercial footprint and advance PearlMatrix through clinical trials.
Nov 2022
Appointed CEO of Cerapedics
Effective November 1, 2022 - investor becomes operator. Retains Chairman role. Begins steering the company through its next commercial phase.
Jun 2025
FDA Approves PearlMatrix
Landmark PMA approval for PearlMatrix P-15 Peptide Enhanced Bone Graft - the first and only proven bone growth accelerator for lumbar fusion. Cerapedics now holds two of only three PMA-approved spinal biologics in the U.S.
Jan 2026
Expanded FDA Indications for PearlMatrix
FDA approves label expansion covering ALIF, PLIF, OLIF, and LLIF approaches - dramatically widening the addressable patient population. Vizient supplier agreement follows, reaching 65%+ of acute care providers.

What She Built

🌟
Two FDA PMAs
Only CEO running a company with two PMA-approved spinal biologics - i-FACTOR (cervical) and PearlMatrix (lumbar). Two of only three such products in the U.S. market.
Regulatory
🧬
150K+ Patients
More than 150,000 patients worldwide have been treated with Cerapedics' P-15 peptide technology. She's scaling a number that was already remarkable when she took the helm.
Patient Impact
📈
2x Fusion Speed
ASPIRE pivotal study: more than twice as many patients achieved lumbar fusion at 6 months with PearlMatrix vs. local autograft. Statistically superior clinical success.
Clinical Evidence
🏢
Vizient Network
Secured supplier agreement with Vizient, covering 65%+ of U.S. acute care providers and 97% of academic medical centers. A distribution reach most medtech companies spend years chasing.
Commercial
📊
$162M Raised
Total funding secured including a $25M venture round. Cerapedics now generates approximately $67M in annual revenue with 230 employees and expanding headquarters in Colorado.
Growth
🎻
5-Board Investor
While at KCK, Schroeder served on boards at Cerapedics, Sight Sciences, Aerin Medical, Intuity Medical, and Lungpacer - spanning spine, eyes, ENT, diabetes, and pulmonary medicine.
Portfolio

Two PMAs. One Company. One CEO.

i-FACTOR
P-15 Peptide Enhanced Bone Graft — Cervical
FDA PMA Approved
Cervical Spine (ACDF)

The original Cerapedics flagship. A P-15 peptide enhanced bone graft approved for single-level anterior cervical discectomy and fusion (ACDF). The product that established Cerapedics' clinical credibility and set the stage for everything that followed.

✓ FDA PMA Approved
PearlMatrix
P-15 Peptide Enhanced Bone Graft — Lumbar
2x Faster fusion vs. autograft
at 6 months (ASPIRE study)

The milestone product. PMA approved June 2025 for lumbar TLIF - the first bone growth accelerator proven to speed lumbar fusion. By January 2026, indications expanded to include ALIF, PLIF, OLIF, and LLIF. The addressable market just got much larger.

✓ FDA PMA Approved — Expanded Jan 2026

Why the P-15 Peptide Is Different

P-15 Peptide — 15 Amino Acid Chain
G
T
P
G
P
Q
G
I
A
G
Q
R
G
V
V
Synthetic sequence mimicking collagen's cell-binding domain

It Activates. It Doesn't Replace.

Most bone graft substitutes work by providing scaffold. The P-15 peptide does something more specific: it mimics a 15-amino-acid binding sequence from Type I collagen that osteogenic cells - the cells responsible for bone formation - naturally latch onto.

When surgeons pack the fusion site with a P-15-enhanced graft, the peptide signals osteogenic cells to attach, proliferate, and differentiate. The body's own repair machinery gets recruited to the exact location where fusion needs to happen.

Thirty years of development produced a technology that's now treated over 150,000 patients. Under Schroeder's leadership, it earned a second FDA PMA in 2025 and expanded indications in 2026. The pipeline is built on the same mechanism across multiple spinal approaches.

30+
Years in Development
15
Amino Acid Sequence
3
Only PMA-Approved Grafts

Three Degrees. One University. One Discipline.

BS
Materials Science & Engineering
UC Berkeley
MS
Materials Science & Engineering
UC Berkeley
Ph.D.
Materials Science & Engineering
UC Berkeley

Three degrees from the same Berkeley program isn't academic inertia - it's a signal about depth over breadth. The foundational understanding of how materials behave at the molecular level informs how she thinks about drug-device combinations, clinical data, and the long arc of regulatory science.

What She Says

"The FDA approval of PearlMatrix Bone Graft is a significant achievement for Cerapedics as we're the only company with two PMA-approved products for use in spinal fusion."
- On the June 2025 PearlMatrix FDA Approval
"We look forward to delivering improved bone repair outcomes for patients, doctors, and payers with our innovative P-15 peptide technology."
- On taking the CEO role, November 2022
"PearlMatrix's spinal fusion product has shown statistically superior fusion speed, and surgeon interest is strong. This contract underscores Cerapedics' commitment to enhance patient care."
- On the Vizient supplier agreement, 2026
"I've been super excited about the Cerapedics story for many years."
- On her long-standing conviction in the company's technology
Former Board Seats at KCK Portfolio Companies
Cerapedics Sight Sciences Aerin Medical Intuity Medical Lungpacer

Numbers Worth Knowing

3
UC Berkeley degrees - all in the same field. BS, MS, and PhD in Materials Science and Engineering from one institution.
6
Years at KCK MedTech as an investor before transitioning to operator at Cerapedics. Patient capital shapes patient thinking.
5
Portfolio company boards at once during her KCK tenure: spanning spine, ophthalmology, ENT, diabetes, and pulmonary medicine.
2/3
Cerapedics holds two of only three FDA PMA-approved spinal biologics available in the United States.
65%
Of U.S. acute care providers now reached through Vizient supplier agreement - including 97% of academic medical centers.
4yr
Time from joining Cerapedics' board (2018) to becoming CEO (2022). She watched, invested, then led. That sequence is deliberate.