Johnson & Johnson Consumer Companies, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Johnson & Johnson Consumer Companies, Inc. makes
The company produces liquid bandages for wound care, including adhesive dressings designed for minor cuts, burns, and skin abrasions, as well as disposable wound drainage tubes for managing fluid from surgical or traumatic injuries.
These products are regulated under FDA Class I and Class II (Unclassified) designations, with some devices requiring 510(k) clearance. The company is headquartered in the United States and its devices are listed in the FDA’s 510(k) registry.
Catalogue
Band-Aid(R) Brand Liquid Bandage Ref K062602
Regimes: 510(k) Registry: 510(k)Freedom, Model 4660 Ref K001023
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Johnson & Johnson Consumer Companies, Inc. have in the registry?
The registry currently lists 2 devices for Johnson & Johnson Consumer Companies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Johnson & Johnson Consumer Companies, Inc.'s devices?
Among its 2 most recently registered devices, Johnson & Johnson Consumer Companies, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Johnson & Johnson Consumer Companies, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Johnson & Johnson Consumer Companies, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Johnson & Johnson Consumer Companies, Inc. in the registry?
The most recently registered devices listed for Johnson & Johnson Consumer Companies, Inc. include BAND-AID(R) BRAND LIQUID BANDAGE and FREEDOM, MODEL 4660.