Medical Device Manufacturer · US , Washington , DC

Kavo America - FDA 510(k) Cleared Devices

20 submissions · 19 cleared · Since 1991

20

Total

19

Cleared

1

Denied

FDA 510(k) Regulatory Record - Kavo America General & Plastic Surgery ✕

4 devices

1-4 of 4

Cleared Jul 10, 2008

KEY LASER III 1243 US WITH DETECT

General & Plastic Surgery · 253d

Cleared Oct 26, 2007

GENTLERAY 980 DIODE LASER SYSTEM

General & Plastic Surgery · 72d

Cleared May 04, 2000

KAVO K.E.Y. LASER 1242

General & Plastic Surgery · 52d

Cleared Jan 27, 1999

KAVO KEY LASER 1242

General & Plastic Surgery · 146d