Plancon Instruments is one of 183 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Plancon Instruments - FDA 510(k) Cleared Devices
Recent clearances: PLANCON MICROLAMELLAR KERATOME EVOLUTION, PLANCON MICROLAMELLAR KERATOME (SINGLE PIECE KERATOME HEAD WITH ACCESSORIES)
3
Total
3
Cleared
0
Denied
Plancon Instruments has 3 FDA 510(k) cleared medical devices. Based in Antony, FR.
Historical record: 3 cleared submissions from 1996 to 1998. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Plancon Instruments Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Plancon Instruments
3 devices