Optimed Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Optimed Technologies, Inc. - FDA 510(k) Cleared Devices
15
Total
15
Cleared
0
Denied
Optimed Technologies, Inc. has 15 FDA 510(k) cleared medical devices. Based in Irvine, US.
Historical record: 15 cleared submissions from 1988 to 1997.
Browse the FDA 510(k) cleared devices submitted by Optimed Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Optimed Technologies, Inc.
15 devices
Cleared
Sep 29, 1997
OPTIVIEW
Radiology
84d
Cleared
Nov 04, 1996
BOOSTER LITE 3 MOTORIZED SCOOTER
Physical Medicine
355d
Cleared
Nov 04, 1996
BOOSTER TROPHY 5 MOTORIZED SCOOTER
Physical Medicine
355d
Cleared
Nov 04, 1996
BOOSTER LITE 4 MOTORIZED SCOOTER
Physical Medicine
355d
Cleared
Oct 18, 1994
FLEXIBLE FIBER OPTIC LAPAROSCOPES
Obstetrics & Gynecology
84d
Cleared
Jul 12, 1994
LAPAROSCOPE, GYNECOLOGIC (AND ACCESSORIES)
Obstetrics & Gynecology
809d
Cleared
Jun 24, 1994
HYSTEROSCOPE (AND ACCESSORIES)
Obstetrics & Gynecology
791d
Cleared
May 17, 1994
FLEXIBLE FIBER OPTIC GYNECOLOGIC ENDOSCOPE
Obstetrics & Gynecology
711d
Cleared
Jun 29, 1993
ARTHROSCOPE & ACCESSORIES
Orthopedic
427d
Cleared
Feb 19, 1993
FLEXIBLE FIBER OPTIC ENDOSCOPE
Gastroenterology & Urology
253d
Cleared
Nov 23, 1992
ENDOSCOPE
Gastroenterology & Urology
216d
Cleared
Sep 14, 1992
FLEXIBLE FIBER OPTIC ENDOSCOPE
Ear, Nose, Throat
88d