Glenroe Technologies is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Glenroe Technologies - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Glenroe Technologies has 8 FDA 510(k) cleared medical devices. Based in Bradenton, US.
Historical record: 8 cleared submissions from 1992 to 1998. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Glenroe Technologies Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Glenroe Technologies
8 devices
Cleared
Feb 24, 1998
GLENROE CHAIN
Dental
49d
Cleared
Jan 27, 1995
GLENROE ORTHO-SIL
Dental
74d
Cleared
Jan 06, 1994
GLENROE ELASTIBITE STIMULATOR
Dental
496d
Cleared
Aug 24, 1993
GLENROE PLASTIC BRACKET
Dental
70d
Cleared
Apr 27, 1993
TUFF TIES
Dental
252d
Cleared
Apr 08, 1993
GLENROE ORTHO SEPS
Dental
233d
Cleared
Mar 31, 1993
EJECTOR
Dental
223d
Cleared
Nov 25, 1992
GLENROE BAND SEATING CONTOURING INSTRUMENT
Dental
55d