Dermatological Research Laboratories, Inc.
Country not established
- Devices
- 1
What Dermatological Research Laboratories, Inc. makes
Dermatological Research Laboratories, Inc. manufactures post-surgical and post-biopsy kits designed for wound care and tissue management following dermatological procedures. These kits include sterile tools and supplies intended to support healing and reduce infection risk in clinical settings.
The company’s products are classified as Class II medical devices under FDA regulations and are authorised through the 510(k) clearance pathway. These devices are listed in the FDA’s 510(k) registry, and the manufacturer operates from the United States.
Catalogue
Post Surgical Kit/Post Biopsy Kit Ref K910011
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dermatological Research Laboratories, Inc. have in the registry?
The registry currently lists 1 device for Dermatological Research Laboratories, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dermatological Research Laboratories, Inc.'s devices?
Among its 1 most recently registered device, Dermatological Research Laboratories, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Dermatological Research Laboratories, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Dermatological Research Laboratories, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dermatological Research Laboratories, Inc. in the registry?
The most recently registered devices listed for Dermatological Research Laboratories, Inc. include POST SURGICAL KIT/POST BIOPSY KIT.