Kemi Labs, Inc.
Country not established
- Devices
- 1
What Kemi Labs, Inc. makes
Kemi Labs, Inc. manufactures the KEMI LABS Adhesive Bandage Remover, a device designed to safely and gently remove adhesive bandages from skin without causing irritation or damage.
The product is classified as a Class I medical device under FDA regulations and is listed in the FDA’s 510(k) clearance database. The company is based in the United States.
Catalogue
Kemi Labs - Adhesive Bandage Remover Ref K895293
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kemi Labs, Inc. have in the registry?
The registry currently lists 1 device for Kemi Labs, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kemi Labs, Inc.'s devices?
Among its 1 most recently registered device, Kemi Labs, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Kemi Labs, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Kemi Labs, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Kemi Labs, Inc. in the registry?
The most recently registered devices listed for Kemi Labs, Inc. include KEMI LABS - ADHESIVE BANDAGE REMOVER.