Medical Device Manufacturer · US , Phoenix , AZ

Dornier Surgical Products, Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1998

Total

Cleared

Denied

Dornier Surgical Products, Inc. has 9 FDA 510(k) cleared medical devices. Based in Phoenix, US.

Historical record: 9 cleared submissions from 1998 to 2001. Primary specialty: General & Plastic Surgery.

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

Dornier Surgical Products, Inc. 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 - Dornier Surgical Products, Inc.

9 devices

1-9 of 9

Cleared Mar 26, 2001

DORNIER MEDILAS D SKINPULSE LASER SYSTEM (SKINPULSE)

K003993 · GEX

General & Plastic Surgery · 90d

Cleared Jun 12, 2000

DORNIER MEDILAS D SKINPULSE

K000072 · GEX

General & Plastic Surgery · 154d

Cleared May 24, 2000

DORNIER MEDILAS H

K001243 · GEX

General & Plastic Surgery · 36d

Cleared Nov 08, 1999

DORNIER SCANNER HANDPIECE

K993146 · GEX

General & Plastic Surgery · 49d

Cleared Jun 09, 1999

DORNIER LASERTRODE FIBER

K991183 · GEX

General & Plastic Surgery · 62d

Cleared Mar 26, 1999

DORNIER MEDILAS H/2

K984591 · GEX

General & Plastic Surgery · 88d

Cleared Sep 14, 1998

DORNIER MEDILAS D

K982629 · GEX

General & Plastic Surgery · 48d

Cleared Jul 20, 1998

DORNIER MEDILAS E

K981438 · GEX

General & Plastic Surgery · 90d

Cleared Jul 17, 1998

DORNIER MEDILAS H

K981718 · GEX

General & Plastic Surgery · 63d

Dornier Surgical Products, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Dornier Surgical Products, Inc.

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