Medical Device Manufacturer · US , Sunnyvale , CA

Coalescent Surgical - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 2000

Total

Cleared

Denied

Coalescent Surgical has 9 FDA 510(k) cleared medical devices. Based in Sunnyvale, US.

Historical record: 9 cleared submissions from 2000 to 2004. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Coalescent Surgical Filter by specialty or product code using the sidebar.

Coalescent Surgical is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Coalescent Surgical

9 devices

1-9 of 9

Cleared Apr 23, 2004

COALESCENT SURGICAL U-CLIP AND ACCESSORIES

K040821 · FZP

General & Plastic Surgery · 24d

Cleared Jul 03, 2003

MODIFICATION TO COALESCENT SURGICAL U-CLIP AND ACCESSORIES

K031623 · FZP

General & Plastic Surgery · 41d

Cleared Jan 17, 2003

COALESCENT SURGICAL U-CLIP AND ACCESSORIES

K024366 · FZP

General & Plastic Surgery · 17d

Cleared Dec 18, 2002

COALESCENT U-CLIP- AND ACCESSORIES

K023125 · NJU

General & Plastic Surgery · 90d

Cleared Jul 03, 2002

COALESCENT SURGICAL U-CLIP - OR OTHER TBD AND ACCESSORIES

K021407 · FZP

General & Plastic Surgery · 61d

Cleared Jan 24, 2002

COALESCENT SURGICAL U-CLIP

K013664 · NCA

General & Plastic Surgery · 79d

Cleared Aug 31, 2001

COALESCENT SURGICAL U-CLIP

K012317 · FZP

General & Plastic Surgery · 39d

Cleared Feb 06, 2001

COALESCENT U-CLIP DELIVERY AND DISPOSAL DEVICE

K003958 · FZP

General & Plastic Surgery · 47d

Cleared Feb 04, 2000

COALESCENT SURGICAL SUTURED-CLIP

K994160 · FZP

General & Plastic Surgery · 57d

Coalescent Surgical - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Coalescent Surgical

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