BREAKING · ForCast Orthopedics  Series A initial close led by OrthoInnovations (Aug 2025)  FC001 holds FDA Orphan Drug + QIDP designation  FC002 holds FDA QIDP designation  KORU Medical partnership powers the WIIS pump  Selected for MedTech Innovator 2026 cohort  Clinical trial targeted for 2026  WIIS is pronounced "wise"
Company Profile / MedTech

ForCast Orthopedics

A four-person team in Denver is trying to fix one of joint replacement's quietest disasters - by sending antibiotics straight into the joint, where the infection actually lives.

Periprosthetic Joint Infection Denver, Colorado Development-stage device co. Series A
ForCast Orthopedics - orthopedic surgery in the company's signature chevron frame

The operating room, framed in ForCast's own forward-pointing chevron. The infection ForCast targets starts in moments like this - and can outlast the surgery by years.

Who they are now

A small company picking a big, ignored fight

Somewhere right now, a joint replacement that went perfectly is failing. Not because the hardware broke, but because bacteria found it, settled in, and built a wall. ForCast Orthopedics exists for that patient. The company is a development-stage drug-device maker in Denver, Colorado, with roughly four employees, two FDA-designated programs, and a single stubborn target: periprosthetic joint infection, or PJI.

It is not a household name. It does not want to be. ForCast's pitch is narrow on purpose - "Pioneering the treatment of joint infection," as the company puts it - and that narrowness is the whole strategy. While the orthopedic industry chases better implants and faster recoveries, ForCast is staring at what happens when those implants get infected, which is a problem most companies would rather leave to the surgeons and the antibiotics. ForCast thinks both of those are losing the fight.

"Modernize the standard of care for periprosthetic joint infections and improve the quality of life for the growing population of joint replacement patients."
- ForCast Orthopedics, stated mission
The problem they saw

Biofilm: the wall antibiotics can't climb

Here is the uncomfortable part. PJI is rare, which is exactly why it gets under-resourced. But when it hits, it is brutal. The infecting bacteria do not just float around the joint - they stick to the prosthesis and form a biofilm, a slimy protective layer that shrugs off the systemic antibiotics coursing through the bloodstream. The drugs arrive, knock politely, and never get in.

So the standard treatment escalates. Often that means a two-stage revision: pull the infected implant, place an antibiotic-loaded cement spacer, wait, then operate again to put a new joint in. Weeks of IV antibiotics. Months of disruption. PJI can threaten the joint's function, the limb itself, and in the worst cases the patient's life. It is, by any honest measure, a treatment built around the limits of the tools, not the needs of the patient.

The antibiotics weren't failing because they were weak. They were failing because they never reached the wall.
- The case for local delivery

ForCast's read on the situation is blunt: flooding the entire body with antibiotics to treat one infected joint is both too much and not enough. Too much for the patient's system. Not enough at the one spot that matters. That gap - between where the drug goes and where the infection lives - is the company's entire reason to exist.

The founders' bet

A surgeon and an entrepreneur walk into a joint

ForCast was built by people who had seen the problem from both ends. Jared Foran, MD, is an orthopedic surgeon and co-founder who serves as the company's chief scientific and medical officer - the person who has actually stood over the failed joints. Peter Noymer, PhD, is a life-sciences entrepreneur and the executive chairman and CEO - the person who knows how to turn a clinical conviction into a regulated product.

Their bet is almost embarrassingly simple: if the infection is local, the treatment should be local too. Deliver targeted, high-concentration antibiotics directly into the infected joint, build up a local reservoir strong enough to disrupt the biofilm, and do it with a device that automates the whole thing rather than asking surgeons to improvise. The bet got a serious vote of confidence in 2025 when Charles A. DeCook, MD - a practicing orthopedic surgeon and serial entrepreneur - led the Series A through his firm OrthoInnovations and joined as chief innovation officer.

Peter Noymer, PhD
Co-Founder · Exec. Chairman & CEO
Jared Foran, MD
Co-Founder · Chief Scientific/Medical Officer
Charles A. DeCook, MD
Chief Innovation Officer · Board
Nick Jozwiak, CFA
Chief Financial Officer
"I believe that his involvement validates the strong potential of the unique treatment approach that we are pioneering."
- Jared Foran, MD, Co-Founder, on Dr. DeCook joining
The product

WIIS, the drug, and the pump

The platform has a name that sounds like advice: WIIS, the Wearable Intra-Articular Infusion System, pronounced "wise." It is a proprietary delivery mechanism that automates infusion of antibiotics directly into the joint space. Rather than relying on a cement spacer to slowly leach drug, WIIS is designed to actively deliver targeted therapy and maintain a local antibiotic reservoir aimed squarely at the biofilm.

Then there are the drugs. ForCast runs two programs, structured to cover the bacterial bases. FC001 uses vancomycin for gram-positive infections; FC002 uses tobramycin for gram-negative ones. Between them, the company wants to handle the organisms most likely to colonize a joint. To make WIIS work as a wearable, ForCast partnered with KORU Medical Systems in September 2025 to integrate KORU's FreedomEDGE infusion pump - the part that actually does the pushing.

Platform

WIIS

Wearable Intra-Articular Infusion System. Automates targeted antibiotic delivery into the infected joint, building a local reservoir to disrupt biofilm. Integrates KORU's FreedomEDGE pump.

Lead Program

FC001

Vancomycin for gram-positive PJI. Holds FDA Orphan Drug and QIDP designations, with eligibility for Fast-Track and Priority Review.

Pipeline

FC002

Tobramycin for gram-negative PJI. Holds FDA QIDP designation. Together with FC001, it aims to cover both halves of the bacterial map.

"After reviewing the entire landscape of infusion pump technologies available, it became clear that KORU's products were best suited for partnering with our WIIS platform."
- Peter Noymer, CEO
Milestones

How a four-person team stacked the regulatory deck

FDA DESIGNATIONS
Orphan Drug + QIDP for FC001, QIDP for FC002
Two programs, both flagged by the FDA as addressing serious, under-served infectious disease - unlocking incentives and a faster regulatory lane.
AUGUST 2025
Initial close of Series A
Led by OrthoInnovations LLC. Charles A. DeCook, MD joins the board and management team as Chief Innovation Officer.
SEPTEMBER 2025
KORU Medical Systems partnership
Agreement to integrate KORU's FreedomEDGE infusion pump into the WIIS platform, supporting a planned clinical trial.
2026 (TARGET)
Clinical trial
The first real test of whether targeted intra-articular delivery can outmaneuver biofilm in patients, not just in theory.
JUNE 2026
MedTech Innovator 2026 cohort
Selected as one of roughly 65 companies from more than 1,800 applicants to the prominent medtech accelerator.
The proof

What's verifiable, and what's still ahead

Let's be skeptical for a second, because ForCast is pre-commercial and the only honest scorecard is the one made of facts. No approved product. No revenue. A clinical trial that hasn't reported. What ForCast does have is a stack of external validation that is harder to fake than a pitch deck: two FDA designations, a Series A led by a working orthopedic surgeon who put his own firm's money in, a named infusion-hardware partner, and a competitive accelerator slot.

The regulatory tailwind

Selected ForCast milestones · counts & selectivity
FDA designations secured
3
Active drug programs
2
Applicants to MTI 2026
1,800+
Companies chosen
~65

Designations counted: Orphan Drug (FC001), QIDP (FC001), QIDP (FC002). Accelerator bars scaled to the applicant pool - roughly a 3.6% acceptance rate.

Three designations. Two programs. One acceptance out of every twenty-eight or so applicants. None of it cures a single patient yet - but all of it is the kind of thing the FDA, an experienced surgeon-investor, and a selective accelerator only hand out when they think the underlying idea is worth the risk.

"ForCast's approach has the potential to deliver best-in-class results for both patients and surgeons."
- Charles A. DeCook, MD, Chief Innovation Officer & lead investor
The mission

Why a rare problem is the right problem

There is an old argument in medtech that you should chase big markets, not rare ones. ForCast is doing the opposite, and on purpose. As joint replacements grow more common across an aging population, the absolute number of PJI cases climbs with them - so a "rare" complication quietly becomes a steady, expensive, life-altering reality for a growing group of people. The Orphan Drug designation exists precisely for this kind of overlooked-but-serious problem.

The company's mission language keeps coming back to "quality of life," which is a tell. ForCast is not really selling a pump or a molecule. It is selling the idea that a patient who develops a joint infection should not have to lose the joint, endure two surgeries, or gamble on systemic drugs that can't reach the target. The mission is to make local, targeted treatment the default instead of the last resort.

Why it matters tomorrow

Back to that failing joint

Return to where we started. A joint replacement that went perfectly is failing because bacteria built a wall the antibiotics can't climb. Today, that patient's most likely future is two surgeries, weeks of IV drugs, and months of their life handed over to a complication nobody warned them about.

ForCast Orthopedics is building the version where that patient gets a wearable pump instead of a second operation - where the drug shows up at the wall in force, not in the bloodstream by chance. None of that is proven yet; the clinical trial is the moment the story either holds or doesn't. But the company has done the unglamorous work of lining up the designations, the money, the hardware partner, and the surgeons who'd actually use it.

If WIIS works, the operating-room scene in that chevron up top stays the same - the surgery still happens, the implant still goes in. What changes is everything that comes after, for the small but growing number of people whose perfect joint quietly turns against them. That is the bet. We'll know more in 2026.

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Video interviews & product demos: none published by the company at the time of writing. Check the website and LinkedIn for the first trial updates.