Biointerface Technologies, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Biointerface Technologies, Inc. makes
Biointerface Technologies, Inc. manufactures transparent wound dressings, including the STERIL-DERM-PLUS and STERIL-DERM products, designed for wound care applications.
These devices are classified under Class I and Class II (U) in the U.S. and are listed via the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Steril-Derm-Plus Transparent Dressing Ref K931766
Regimes: 510(k) Registry: 510(k)Steril-Derm Transparent Wound Dressing Ref K892837
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Biointerface Technologies, Inc. have in the registry?
The registry currently lists 2 devices for Biointerface Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Biointerface Technologies, Inc.'s devices?
Among its 2 most recently registered devices, Biointerface Technologies, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Biointerface Technologies, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Biointerface Technologies, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Biointerface Technologies, Inc. in the registry?
The most recently registered devices listed for Biointerface Technologies, Inc. include STERIL-DERM-PLUS TRANSPARENT DRESSING and STERIL-DERM TRANSPARENT WOUND DRESSING.