Medical Device Manufacturer · US , Palo Alto , CA

Coapt Systems, Inc. - FDA 510(k) Cleared Devices

17 submissions · 17 cleared · Since 2002

Total

Cleared

Denied

Coapt Systems, Inc. has 17 FDA 510(k) cleared medical devices. Based in Palo Alto, US.

Historical record: 17 cleared submissions from 2002 to 2009. Primary specialty: Orthopedic.

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

FDA 510(k) Regulatory Record - Coapt Systems, Inc.

17 devices

1-12 of 17

Cleared Sep 11, 2009

VF LIQUIGEL

K083783 · MIX

Ear, Nose, Throat · 266d

Cleared Apr 25, 2008

MODIFICATION TO VF GEL PLUS

K080956 · MIX

Ear, Nose, Throat · 22d

Cleared Feb 15, 2008

VF GEL PLUS

K071663 · MIX

Ear, Nose, Throat · 242d

MODIFICATION TO ENDOTINE RIBBON

K060828 · GAM

General & Plastic Surgery · 23d

Cleared Jun 23, 2005

ENDOTINE RIBBON

K051415 · GAM

General & Plastic Surgery · 22d

Cleared Apr 06, 2005

ENDOTINE RIBBON

K050611 · GAM

General & Plastic Surgery · 28d

Cleared Nov 05, 2004

ENDOTINE TRANSBLEPH 3.0/3.5 DEVICE

K042796 · HWC

Orthopedic · 29d

Cleared Sep 28, 2004

ENDOTINE MIDFACE B 4.5 DEVICE

K041835 · HWC

General & Plastic Surgery · 83d

Cleared Aug 27, 2004

ENDOTINE FOREHEAD TRIPLE DEVICE

K042078 · HWC

Orthopedic · 25d

Cleared May 10, 2004

ENDOTINE TRANSBLEPH DEVICE

K040740 · HWC

Orthopedic · 49d

Coapt Systems, Inc. - FDA 510(k) Cleared Devices

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