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Company · US

Sterling Drug, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1978 to 1990. Name variants (Inc, Corp, punctuation) are merged.

9510(k) clearances (0 in 12 months)

0recalls (0 in 12 months)

0recalls that name a 510(k)

Product codes

Code	Device	Records
LYC	Bone Grafting Material, Synthetic	3
KGN	Wound Dressing With Animal-Derived Material(S)	2
DZE	Implant, Endosseous, Root-Form	1
FMF	Syringe, Piston	1
FMI	Needle, Hypodermic, Single Lumen	1
JTQ	Bath, Incubators/Water, All	1

Latest 510(k) clearances

Decided	510(k)	Device and applicant	Code
Jun 5, 1990	K901369	GREEN LABEL BIOBRANE II AND RED LABEL BIOBRANE II Sterling Drug, Inc.	KGN
Nov 28, 1989	K896110	BIOBRANE(R) II Sterling Drug, Inc.	KGN
Jan 27, 1988	K875275	WINTHROP PHARMACEUTICALS CONTRAST MEDIA WARMER Sterling Drug, Inc.	JTQ
Apr 5, 1984	K840260	PERIOGRAF DURAPATITE 40-60 MESH Sterling Drug, Inc.	LYC
Feb 24, 1982	K820164	EMPTY STERILE CARPUJECT Sterling Drug, Inc.	FMF
Feb 24, 1982	K820023	CONAGRAF TM DURAPATITE CONES Sterling Drug, Inc.	LYC
Jan 5, 1982	K813257	ALVEOGRAF DURAPATITE(18-40 MESH) Sterling Drug, Inc.	DZE
Nov 20, 1981	K813070	PERIOGRAF Sterling Drug, Inc.	LYC
Apr 10, 1978	K780209	DILUTION SPIKE Sterling Drug, Inc.	FMI

Latest recalls

Date	Firm and product	Code	Linked 510(k)
No recalls in this window.

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