Hall-Woodroof, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Hall-Woodroof, Inc. makes
Hall-Woodroof, Inc. manufactures BIOBRANE BRAND TEMPORARY WOUND DRESSING, a temporary wound dressing used for medical applications.
The company is based in the US and its devices are listed in the FDA 510(k) registry under device class U, which indicates unclassified devices.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Biobrane Brand Temporary Wound Dressing Ref K791184
Regimes: 510(k) Registry: 510(k)Biobrane Brand Temporary Wound-Dressing Ref K801635
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hall-Woodroof, Inc. have in the registry?
The registry currently lists 2 devices for Hall-Woodroof, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hall-Woodroof, Inc.'s devices?
Among its 2 most recently registered devices, Hall-Woodroof, Inc. has devices listed in FDA 510(k) (2 devices).
What are the newest devices from Hall-Woodroof, Inc. in the registry?
The most recently registered devices listed for Hall-Woodroof, Inc. include BIOBRANE BRAND TEMPORARY WOUND DRESSING and BIOBRANE BRAND TEMPORARY WOUND-DRESSING.