Company · US

Teledyne Getz

FDA 510(k) clearances and medical device recalls filed under this name, 1990 to 1992. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)

0recalls (0 in 12 months)

0recalls that name a 510(k)

Product codes

Code	Device	Records
EJR	Agent, Polishing, Abrasive, Oral Cavity	2
EFB	Handpiece, Air-Powered, Dental	1
KOB	Catheter, Suprapubic (And Accessories)	1
KOT	Carboxymethylcellulose Sodium Or Polyvinyl Methylether Maleic Acid Calcium-Sodium	1

Decided	510(k)	Device and applicant	Code
Nov 5, 1992	K923675	DENSPRO MEDIUM MINT PROPHY PASTE Teledyne Getz	EJR
Nov 5, 1992	K923674	DENSPRO COARSE MINT PROPHY PASTE Teledyne Getz	EJR
Oct 24, 1990	K903568	SUPER STRENGTH DENTURE ADHESIVE CREAM Teledyne Getz	KOT
Jun 6, 1990	K901938	SUPER STRENGTH DENTURE ADHESIVE CREAM Teledyne Getz	KOB
May 15, 1990	K901239	TELEDYNE GETZ'S DISPOSABLE PROPHY ANGLE Teledyne Getz	EFB

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