Collamatrix Co., Inc.
TaiwanFDA applicant, unverified
- Devices
- 6
What Collamatrix Co., Inc. makes
Collamatrix Co., Inc. manufactures wound care products, including collagen-based dressings and hydrogels designed for skin repair and wound management. Their portfolio includes modifications of collagen dressings, standard collagen wound dressings, and collagen-based hydrogels intended for topical application.
These devices are classified as Class II under FDA regulations and are authorised via the 510(k) pathway. The company’s products are listed in the FDA’s 510(k) registry. Collamatrix Co., Inc. is based in the United States.
Catalogue
Modification To Collawound Dressing Ref K070269
Regimes: 510(k) Registry: 510(k)Collawound Art Ref K093351
Regimes: 510(k) Registry: 510(k)Collawound Hydrogel Ref K071557
Regimes: 510(k) Registry: 510(k)Colladental Barrier Ref K100695
Regimes: 510(k) Registry: 510(k)Collawound Wound Dressing Ref K090894
Regimes: 510(k) Registry: 510(k)Collawound Dressing Ref K061474
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Collamatrix Co., Inc. have in the registry?
The registry currently lists 6 devices for Collamatrix Co., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Collamatrix Co., Inc.'s devices?
Among its 6 most recently registered devices, Collamatrix Co., Inc. has devices listed in FDA 510(k) (6 devices).
What risk classes do Collamatrix Co., Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Collamatrix Co., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Collamatrix Co., Inc. in the registry?
The most recently registered devices listed for Collamatrix Co., Inc. include MODIFICATION TO COLLAWOUND DRESSING, COLLAWOUND ART, COLLAWOUND HYDROGEL and COLLADENTAL BARRIER.