Company · US

Ruggles Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 1989 to 1991. 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
GWO	Plate, Cranioplasty, Preformed, Alterable	1
HAO	Instrument, Surgical, Non-Powered	1
HBG	Drills, Burrs, Trephines & Accessories (Manual)	1
LXH	Orthopedic Manual Surgical Instrument	1
LYQ	Accessories, Fixation, Spinal Intervertebral Body	1

Decided	510(k)	Device and applicant	Code
Feb 21, 1991	K903485	TITANIUM MESH Ruggles Corp.	GWO
Sep 20, 1990	K902818	MULTIPLE NONPOWERED NEUROSURGICAL INSTRUMENT Ruggles Corp.	HBG
Aug 9, 1990	K902819	LAMINECTOMY ROGEUR Ruggles Corp.	LXH
Jul 18, 1990	K902850	ZEPPELIN INSTRUMENTS Ruggles Corp.	HAO
Jun 7, 1989	K893415	TRANS-ORAL DEPTH GAUGE Ruggles Corp.	LYQ

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