Bioresorbable by design
Silk-based implants can be tuned to provide mechanical support, then safely resorb — avoiding the second surgeries and stress‑shielding associated with permanent metal hardware.
SilkMatrix™ transforms silk fibroin and sericin into bioresorbable implants and matrices for bone repair, dental regeneration, wound care and tissue engineering.
Silk sutures have been trusted in surgery for over a century. But regenerated silk fibroin and sericin — tunable, bioresorbable, and biocompatible — are only beginning to reach the clinic. SilkMatrix is built to close that gap with an indigenous, scalable platform.
Silk-based implants can be tuned to provide mechanical support, then safely resorb — avoiding the second surgeries and stress‑shielding associated with permanent metal hardware.
One core material science enables many devices — fixation, dental membranes, wound matrices, scaffolds and coatings — multiplying shots on goal from a single R&D base.
India is a leading producer of silk. SilkMatrix aims to convert that raw-material advantage into high-value, indigenous regenerative medical devices.
Our platform processes silk fibroin and sericin into purified, controllable biomaterials — films, gels, porous scaffolds, coatings and solid forms — with tunable strength and resorption profiles.
Our first focused program develops a silk-based screw and plate system for fracture fixation — verified through mechanical testing, ISO 10993 biological evaluation, and small- and large-animal preclinical studies.
It is the most de-risked path to first revenue and clinical credibility for the broader platform.
Inside the lead program →The lead program is grounded in the founder’s own research, where he demonstrated that a silk-fibroin cryogel can meet bone-fixation requirements, with compressive strength comparable to human bone. He then became an ISO 10993 biocompatibility expert — the exact skill needed to turn proven science into an approved device. SilkMatrix builds its own, independently-owned IP from there.
Demonstrated a silk-cryogel construct with bone-like strength, meeting bone-fixation requirements in his own graduate research.
Runs a regulatory practice preparing biological evaluations for EU MDR, FDA & CDSCO.
Implant biocompatibility research at INSERM, France (EU Horizon 2020).
10+ years in biomaterials & cell biology; peer-reviewed author (Elsevier, Wiley).
A staged pipeline: prove the platform with the lead fixation program, then expand into adjacent high-value regenerative markets.
Bioresorbable bone fixation — screws & plates.
Porous scaffolds for soft & hard tissue engineering.
Advanced wound-healing matrices & dressings.
Guided bone regeneration & dental membranes.
Bioactive silk coatings for implant surfaces.
We structure investment so capital is deployed against evidence — each phase ends in an explicit Go / No-Go decision before the next is committed.
Prove reproducibility, formulation, early safety, and IP / legal readiness.
Develop the screw / plate system, verify mechanics, and complete biological & animal validation.
We are engaging a select group of strategic investors and technical advisors to build the indigenous silk biomaterials platform. Request the full confidential brief.