Dermtec, Inc.
Country not established
- Devices
- 1
What Dermtec, Inc. makes
Dermtec, Inc. manufactures disposable curettes, which are handheld surgical instruments used for scraping or debriding skin lesions, wounds, or other tissue surfaces in clinical settings.
The company’s disposable curette is classified as a Class I medical device under FDA regulations and is listed via the 510(k) pathway. The product is based in the United States.
Catalogue
Disposable Curette Ref K921022
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dermtec, Inc. have in the registry?
The registry currently lists 1 device for Dermtec, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dermtec, Inc.'s devices?
Among its 1 most recently registered device, Dermtec, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Dermtec, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Dermtec, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Dermtec, Inc. in the registry?
The most recently registered devices listed for Dermtec, Inc. include DISPOSABLE CURETTE.