Plancon Instruments
FranceFDA applicant, unverified
- Devices
- 3
What Plancon Instruments makes
Plancon Instruments manufactures ophthalmic surgical devices, specifically microlamellar keratomes, which are used in eye surgery procedures. Their product line includes the Plancon Microlamellar Keratome, Plancon Mircolamellar Keratome, and Plancon Microlamellar Keratome Evolution, along with accessories for these devices.
The company's devices are classified as Class I and are listed in the FDA 510(k) registry. Plancon Instruments is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Plancon Mircolamellar Keratome Ref K960395
Regimes: 510(k) Registry: 510(k)Plancon Microlamellar Keratome Evolution Ref K980924
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Plancon Instruments have in the registry?
The registry currently lists 3 devices for Plancon Instruments. Devices recorded under merged duplicate company entries are counted once.
Which registries list Plancon Instruments's devices?
Among its 3 most recently registered devices, Plancon Instruments has devices listed in FDA 510(k) (3 devices).
What risk classes do Plancon Instruments's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Plancon Instruments's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Plancon Instruments in the registry?
The most recently registered devices listed for Plancon Instruments include PLANCON MICROLAMELLAR KERATOME (SINGLE PIECE KERATOME HEAD WITH ACCESSORIES), PLANCON MIRCOLAMELLAR KERATOME and PLANCON MICROLAMELLAR KERATOME EVOLUTION.