Woodroof Laboratories, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Woodroof Laboratories, Inc. makes
Woodroof Laboratories, Inc. manufactures temporary wound dressings, including a silicone-based barrier film designed to protect wounds from infection and moisture loss, as well as an adhesive-backed version for secure application to skin.
These products are classified as Class II devices under FDA regulations and are listed via the 510(k) clearance process. The company operates from the United States.
Catalogue
Biobrane Brand Temporary Wound Dressing Ref K790496
Regimes: 510(k) Registry: 510(k)Biobrane Brand Temp. Wound Dressing W/Adhesive Ref K844052
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Woodroof Laboratories, Inc. have in the registry?
The registry currently lists 2 devices for Woodroof Laboratories, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Woodroof Laboratories, Inc.'s devices?
Among its 2 most recently registered devices, Woodroof Laboratories, Inc. has devices listed in FDA 510(k) (2 devices).
What are the newest devices from Woodroof Laboratories, Inc. in the registry?
The most recently registered devices listed for Woodroof Laboratories, Inc. include BIOBRANE BRAND TEMPORARY WOUND DRESSING and BIOBRANE BRAND TEMP. WOUND DRESSING W/ADHESIVE.