Medical Device Manufacturer · US , Park Forest , IL

Adri - FDA 510(k) Cleared Devices

6 submissions · 5 cleared · Since 1987

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.

6 devices

1–6 of 6

SILVERSITE OR CALGITROL

K041268 · MGQ Dressing, Wound And Burn, Hydrogel W/drug And/or Biologic · General & Plastic Surgery

CALGITROL AG SILVER ALGINATE WOUND DRESSING

K011618 · FRO Dressing, Wound, Drug · General & Plastic Surgery

FOAM CALCIUM ALGINATE TOPICAL WOUND DRESSING WITH COLLAGEN

K000054 · KGN Wound Dressing With Animal-derived Material(s) · General & Plastic Surgery

FOAM CALCIUM ALIGINATE TOPICAL WOUND DRESSING

K963656 · KMF Bandage, Liquid · General & Plastic Surgery

ALGINATE FIBER TOPICAL WOUND DRESSING

K940404 · KMF Bandage, Liquid · General & Plastic Surgery

ALGINATE WOOL FIBER

K870383 · KHR Absorber, Saliva, Paper · Dental