Westaim Biomedical, Inc.
United StatesFDA applicant, unverified
- Devices
- 6
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Acticoat Foam Dressing Ref K000051
Regimes: 510(k) Registry: 510(k)Acticoat 7 Dressing Ref K001519
Regimes: 510(k) Registry: 510(k)Acticoat Primary Antimicrobial Dressing Ref K992221
Regimes: 510(k) Registry: 510(k)Acticoat Composite Dressing Ref K002466
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Modification To Acticoat Foam Dressing Ref K010447
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Westaim Biomedical, Inc. have in the registry?
The registry currently lists 6 devices for Westaim Biomedical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Westaim Biomedical, Inc.'s devices?
Among its 6 most recently registered devices, Westaim Biomedical, Inc. has devices listed in FDA 510(k) (6 devices).
What risk classes do Westaim Biomedical, Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Westaim Biomedical, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Westaim Biomedical, Inc. in the registry?
The most recently registered devices listed for Westaim Biomedical, Inc. include ACTICOAT FOAM DRESSING, ACTICOAT 7 DRESSING, ACTICOAT PRIMARY ANTIMICROBIAL DRESSING and ACTICOAT COMPOSITE DRESSING.