Medical Device Manufacturer · US , Mchenry , IL

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

9 submissions · 9 cleared · Since 1978

9

Total

9

Cleared

0

Denied

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

4 devices

1-4 of 4

Cleared Apr 05, 1984

PERIOGRAF DURAPATITE 40-60 MESH

Cleared Feb 24, 1982

CONAGRAF TM DURAPATITE CONES

Cleared Jan 05, 1982

ALVEOGRAF DURAPATITE(18-40 MESH)

Cleared Nov 20, 1981