Partner with unmatched quality and expertise
Best-In-Class Biomaterial
See how our medical grade collagen is the precise biomaterial you need.
Product Development
From concept to commercialization — our experience equals your commercial success.
Contract Manufacturing
See why so many companies trust Collagen Matrix as their go-to manufacturing partner.
Put our medical grade collagen in your product
With TruSource™ medical grade collagen, the biomaterial in your product meets the highest standards. TruSource is a highly purified, implantable biomaterial that includes vital properties to support the body’s natural ability to regenerate and serves a broad spectrum of clinical applications. TruSource guarantees the highest level of biomaterial quality to enable peak performance from your finished product. Our long history of service excellence, consistent supply, quality and regulatory acumen ensures speed and success.
Our proprietary processing technique and 20+ years of unparalleled expertise mean your products are built with a level of quality you cannot achieve anywhere else.
Orthopedic, Spine, Vascular, Sports Medicine, Wound Care, Hemostats, Drug Delivery, and more – whatever your need, we have the know-how.
Unmatched Type-1 Collagen Purity
- Highly purified for biocompatibility
- 100% resorbable through normal metabolic pathways
- Intrinsic hemostatic properties control minor bleeding
- Well-established, long clinical history
- Retains biological factors
Technical Specifications
ASTM F2212-19 Characterization
ISO 22442-1, ISO 22442-2 & ISO 22442-3 Compliance
- Isolated and purified from safe xenograft source
- Hydroxyproline >12%
- SDS PAGE Characterization
- Insoluble Collagen
- Hexosamine Content ≤ 0.10%
- LAL Endotoxin Level
- Total Bioburden
- Heavy Metal Content
- Available as Dry Powder or Collagen Sheets
- Various particle sizes available
- Moisture Content <15%
- Shelf Life – 36 months
- Room Temperature Storage
Whatever your needs, we have the biomaterials to match them.
Looking for a development partner?
Our experience equals your commercial success.
Design and development, prototyping, pre-clinical and clinical testing, regulatory filing, manufacturing – in the world of regenerative medicine, each step must be seamless. Your success depends on it. Lack of expertise leads to headaches, unexpected delays, lost market share, and financial benchmarks missed.
Expertise across all steps to commercialization
Design
Requirements
Design and
Development Plan
Product
Development
Pre-clinical and
Clinical Testing
Regulatory Filing
Design Transfer and
Commercialization
Design
Requirements
Product
Development
Regulatory Filing
Design and
Development Plan
Pre-clinical and
Clinical Testing
Design Transfer and
Commercialization
Product applications across all areas of regenerative medicine
Our proprietary technology offering
Extremely diverse technology with broad medical applications
Tissue-like feel, high mechanical strength
Resorption and bone remodeling profile homologous to that of natural human bone
Superior handling characteristics, flexible design parameters
Ability to deposit a thin layer on multiple materials to modify the surface for bioactivity, biocompatibility, hemostasis, cell adhesion, etc.
Single or multi-layered, molded or non-woven, resorbable synthetic polymer matrix with control of porosity, strength
You have the vision of what you want to achieve –
we have the capability to bring it to life.
Looking for a manufacturing partner?
Take a look at our capabilities.
When it comes to manufacturing, our state-of-the-art facilities, expertise, and broad range of capabilities make us the ideal choice to meet your evolving needs. We bring precision and rigor to every step to ensure your end product is of impeccable quality.
We offer state-of-the-art Class 10,000 (ISO Class 7) controlled environments.
And our 19,000-square-foot clean room and 37,000-square-foot manufacturing areas mean that we are able to scale up right away to meet your needs on your timeline.
Our established compliance and regulatory certifications make us an ideal partner no matter what your global aspirations.
- Registered FDA medical device manufacturer
- FDA 21CFR 820 quality system regulation compliance
- ISO 22442 compliance
- MDSAP certified
- ISO 13485 certified
Our broad range of capabilities means we are able to meet every aspect of your manufacturing needs with a single, expert partner.
- Process development and validation
- Packaging design and validation
- Sterilization validation
- Shipping simulation studies
- Environmental storage studies
- Shelf-life studies
- Labeling
- Storage
- Distribution
Whatever your needs, we have the capabilities to match them.