S.C.M.D. Keratomes of Arizona
Country not established
- Devices
- 1
What S.C.M.D. Keratomes of Arizona makes
S.C.M.D. Keratomes of Arizona manufactures the SCMD Keratome, a surgical device used for creating precise corneal incisions in refractive eye procedures such as LASIK or corneal transplants.
The company’s portfolio is regulated under FDA’s Class I device classification, with the SCMD Keratome authorised via the 510(k) pathway. The device is listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Scmd Keratome Ref K935342
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does S.C.M.D. Keratomes of Arizona have in the registry?
The registry currently lists 1 device for S.C.M.D. Keratomes of Arizona. Devices recorded under merged duplicate company entries are counted once.
Which registries list S.C.M.D. Keratomes of Arizona's devices?
Among its 1 most recently registered device, S.C.M.D. Keratomes of Arizona has devices listed in FDA 510(k) (1 device).
What risk classes do S.C.M.D. Keratomes of Arizona's devices fall under?
Among its 1 most recently registered device, the classes recorded for S.C.M.D. Keratomes of Arizona's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from S.C.M.D. Keratomes of Arizona in the registry?
The most recently registered devices listed for S.C.M.D. Keratomes of Arizona include SCMD KERATOME.