Kavo America
Kavo America holds FDA 510(k) medical device clearances, first cleared 1991, most recent 2008.
Top product codes for Kavo America
Recent clearances by Kavo America
- K073074 — KEY LASER III 1243 US WITH DETECT
- K072262 — GENTLERAY 980 DIODE LASER SYSTEM
- K063624 — KAVO EVEREST C-TEMP
- K051909 — DIAGNODENT
- K030146 — KAVO KEY LASER 1242 AND KAVO KEY LASER 1243+
- K050019 — IN EXAM INTRAORAL DENTAL X-RAY SYSTEM
- K032081 — KAVO EVEREST ZS-BLANK MODELS, 42, 20, AND 60
- K031868 — PROPHYPEARLS
- K030607 — KAVO EVEREST G-BLANK, KAVO EVEREST G-CERAM, COATING CERAMIC LF-3-PFM, GLAZE AND COLORINGS/STAINING/SHADES
- K024214 — KAVO EVEREST TITANBLANK
- K012308 — KAVO QUATTROCARE
- K013500 — KAVO POLYLUX II
- K002708 — KAVO CORUND HANDPIECE 2013
- K000805 — KAVO K.E.Y. LASER 1242
- DEN990002 — KAVO DIAGNODENT
- K983100 — KAVO KEY LASER 1242
- K973876 — PROPHYFLEX 2, MODEL 2012
- K940950 — KAVO SYSTEMATICA 1060
- K934783 — KAVO INTRASEPT 905
- K910789 — KAVOKLAVE STEAM AUTOCLAVE
Data sourced from openFDA. This site is unofficial and independent of the FDA.