Medical Device Manufacturer · US , Hicksville , NY

Air Techniques, Inc. - FDA 510(k) Cleared Devices

18 submissions · 18 cleared · Since 1995

Total

Cleared

Denied

Air Techniques, Inc. has 18 FDA 510(k) cleared medical devices. Based in Hicksville, US.

Historical record: 18 cleared submissions from 1995 to 2019. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by Air Techniques, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Air Techniques, Inc.

18 devices

1-12 of 18

Cleared Aug 21, 2019

ScanX Touch/ScanX Duo Touch

K191623 · MUH

Radiology · 64d

Cleared Jul 26, 2019

ScanX Barrier Envelopes

K190949 · PEM

General & Plastic Surgery · 106d

Cleared Aug 03, 2010

SCANX D5000 SERIES SCANNER MODEL: D5000-F, D5000-FB, D5000-FVB, D5000-Q,...

K101289 · MQB

Radiology · 88d

Cleared Aug 18, 2009

SPECTRA FLUORESCENCE CARIES DETECTION DEVICE

Air Techniques, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) cleared devices by Air Techniques, Inc.

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