Medical Device Manufacturer · US , Washington , DC

Kavo America - FDA 510(k) Cleared Devices

20 submissions · 19 cleared · Since 1991

Recent clearances: KEY LASER III 1243 US WITH DETECT, GENTLERAY 980 DIODE LASER SYSTEM, KAVO EVEREST C-TEMP

Total

Cleared

Denied

Kavo America has 19 FDA 510(k) cleared dental devices. Based in Washington, US.

Historical record: 19 cleared submissions from 1991 to 2008.

Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.

Kavo America is one of 13831 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Kavo America

20 devices

1-12 of 20

Cleared Jul 10, 2008

KEY LASER III 1243 US WITH DETECT

K073074 · GEX

General & Plastic Surgery · 253d

Cleared Oct 26, 2007

GENTLERAY 980 DIODE LASER SYSTEM

K072262 · GEX

General & Plastic Surgery · 72d

KAVO KEY LASER 1242 AND KAVO KEY LASER 1243+

K030146 · NVK

Dental · 931d

Cleared Jan 31, 2005

IN EXAM INTRAORAL DENTAL X-RAY SYSTEM

K050019 · EHD

Radiology · 26d

Cleared Jul 24, 2003

KAVO EVEREST ZS-BLANK MODELS, 42, 20, AND 60

KAVO EVEREST G-BLANK, KAVO EVEREST G-CERAM, COATING CERAMIC LF-3-PFM, GLAZE...

K030607 · EIH

Dental · 65d

Cleared Mar 12, 2003

KAVO EVEREST TITANBLANK

Kavo America - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Kavo America

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