Medical Device Manufacturer · US , Park Forest , IL

Adri - FDA 510(k) Cleared Devices

6 submissions · 5 cleared · Since 1987

Recent clearances: SILVERSITE OR CALGITROL, CALGITROL AG SILVER ALGINATE WOUND DRESSING, FOAM CALCIUM ALGINATE TOPICAL WOUND DRESSING WITH COLLAGEN

View 6 510(k) Devices ↓

6

Total

5

Cleared

0

Denied

Adri has 5 FDA 510(k) cleared medical devices. Based in Park Forest, US.

Historical record: 5 cleared submissions from 1987 to 2004. Primary specialty: General & Plastic Surgery.

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

Adri is one of 23312 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Adri

6 devices

1-6 of 6

Cleared Sep 20, 2004

SILVERSITE OR CALGITROL

General & Plastic Surgery · 131d

Cleared Nov 15, 2002

CALGITROL AG SILVER ALGINATE WOUND DRESSING

General & Plastic Surgery · 539d

Cleared Mar 13, 2000

FOAM CALCIUM ALGINATE TOPICAL WOUND DRESSING WITH COLLAGEN

General & Plastic Surgery · 66d

Cleared Nov 12, 1996

FOAM CALCIUM ALIGINATE TOPICAL WOUND DRESSING

General & Plastic Surgery · 61d

Cleared May 04, 1994

ALGINATE FIBER TOPICAL WOUND DRESSING

General & Plastic Surgery · 97d

Cleared Apr 30, 1987

ALGINATE WOOL FIBER