Gm Engineering, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Gm Engineering, Inc. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Gm Engineering, Inc. has 11 FDA 510(k) cleared medical devices. Based in La Verne, US.
Historical record: 11 cleared submissions from 1993 to 1995.
Browse the FDA 510(k) cleared devices submitted by Gm Engineering, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Gm Engineering, Inc.
11 devices
Cleared
Sep 12, 1995
ARTICULATING RETRACTOR TISSUE RETRACTORS
General & Plastic Surgery
57d
Cleared
May 30, 1995
CONTINUOUS FLOW BIOPSY PROBE
Gastroenterology & Urology
362d
Cleared
Jan 26, 1995
BERNSTEIN(TM) UTERINE MANIPULATOR
Obstetrics & Gynecology
618d
Cleared
Aug 23, 1994
GM OPTI*CAM CAMER WITH DENTAL FIBER OPTIC LIGHT
Ear, Nose, Throat
140d
Cleared
Aug 19, 1994
GM REUSABLE AND DISPOSABLE TROCAR AND GM REUSABLE AND DISPOSABLE ULTRA-LIGHT...
General & Plastic Surgery
72d
Cleared
Jul 20, 1994
GM OPTI*CAM CAMERA WITH ENT FIBER OPTIC LIGHT
Ear, Nose, Throat
106d
Cleared
May 24, 1994
GM OPTI*CAM CAMERA WITH FIBER OPTIC LIGHT
Ophthalmic
49d
Cleared
Feb 25, 1994
GM CONTINUOUS FLOW BIOPSY PROBE
Gastroenterology & Urology
196d
Cleared
Dec 01, 1993
TRUE FLOW(TM) VALVE
General & Plastic Surgery
299d
Cleared
Dec 01, 1993
GM MONOPOLAR/FRAZIER SUCTION PROBE
General & Plastic Surgery
105d
Cleared
Aug 30, 1993
GM SWIVEL VIDEO (TM) IRRIGATOR
Ear, Nose, Throat
164d