Biomet Merck GmbH
SwitzerlandFDA applicant, unverified
- Devices
- 1
What Biomet Merck GmbH makes
Biomet Merck GmbH manufactures Topkin Wound Dressings, a category of Class U (Class II in the U.S.) medical devices designed for wound care and management. These dressings are intended to promote healing by maintaining a moist wound environment and protecting against infection.
The company’s portfolio is regulated under the FDA’s 510(k) pathway in the United States, where these devices are classified as Class II. The products are listed in the FDA’s 510(k) database, adhering to U.S. medical device regulations. The manufacturer is based in the United States.
Catalogue
Topkin Wound Dressing Ref K031684
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Biomet Merck GmbH have in the registry?
The registry currently lists 1 device for Biomet Merck GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Biomet Merck GmbH's devices?
Among its 1 most recently registered device, Biomet Merck GmbH has devices listed in FDA 510(k) (1 device).
What are the newest devices from Biomet Merck GmbH in the registry?
The most recently registered devices listed for Biomet Merck GmbH include TOPKIN WOUND DRESSING.