Medical Device Manufacturer · US , Mchenry , IL

Sterling Drug, Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1978

Total

Cleared

Denied

Sterling Drug, Inc. has 9 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 9 cleared submissions from 1978 to 1990. Primary specialty: Dental.

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

Sterling Drug, 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 - Sterling Drug, Inc.

9 devices

1-9 of 9

Cleared Jun 05, 1990

GREEN LABEL BIOBRANE II AND RED LABEL BIOBRANE II

K901369 · KGN

General & Plastic Surgery · 74d

Cleared Nov 28, 1989

BIOBRANE(R) II

K896110 · KGN

General & Plastic Surgery · 36d

Cleared Jan 27, 1988

WINTHROP PHARMACEUTICALS CONTRAST MEDIA WARMER

K875275 · JTQ

Microbiology · 34d

Cleared Apr 05, 1984

PERIOGRAF DURAPATITE 40-60 MESH

K840260 · LYC

Dental · 86d

Cleared Feb 24, 1982

CONAGRAF TM DURAPATITE CONES

K820023 · LYC

Dental · 50d

Cleared Feb 24, 1982

EMPTY STERILE CARPUJECT

K820164 · FMF

General Hospital · 35d

Cleared Jan 05, 1982

ALVEOGRAF DURAPATITE(18-40 MESH)

General Hospital · 63d

Sterling Drug, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Sterling Drug, Inc.

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