Medical Device Manufacturer · US , Walker , MI

Genesis Industries, Inc. - FDA 510(k) Cleared Devices

17 submissions · 17 cleared · Since 1983

Recent clearances: ESP FOUR WELL TISSUE CULTURE PLATE, ESP SIX WELL TISSUE CULTURE PLATE, ESP MICRO SIX WELL TISSUE CULTURE PLATE, ESP WELL, EVERT-IT, NOVO VIVO MODEL #17140 AND #17135

Total

Cleared

Denied

Genesis Industries, Inc. has 17 FDA 510(k) cleared dental devices. Based in Walker, US.

Historical record: 17 cleared submissions from 1983 to 2000.

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

Genesis Industries, Inc. is one of 14114 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Genesis Industries, Inc.

17 devices

1-17 of 17

Cleared Feb 18, 2000

ESP FOUR WELL TISSUE CULTURE PLATE, ESP SIX WELL TISSUE CULTURE PLATE, ESP...

K994361 · MQK

Obstetrics & Gynecology · 53d

Cleared Feb 10, 1997

EVERT-IT

K962828 · HGY

Obstetrics & Gynecology · 206d

Cleared Apr 04, 1988

NOVO VIVO MODEL #17140 AND #17135

K880377 · GAA

General & Plastic Surgery · 68d

Cleared Feb 16, 1988

NOVO VIVO SUCTION CATHETER VESSEL W/MUCOSE TRAP

K880376 · GBS

General & Plastic Surgery · 20d

C & B 40 PENTRO C & B40

C & B 61 PENTRON C & B61

C & B57 PENTRON C & B57

Genesis Industries, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Genesis Industries, Inc.

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