Flexmedics - FDA 510(k) Cleared Devices
20
Total
20
Cleared
0
Denied
Flexmedics has 20 FDA 510(k) cleared medical devices. Based in Minneapolis, US.
Historical record: 20 cleared submissions from 1986 to 1999. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Flexmedics Filter by specialty or product code using the sidebar.
20 devices
Cleared
Mar 15, 1999
FLEXFINDER GUIDE WIRE(REGULAR SHAFT/STIFF SHAFT) MARKED INK BANDS, FLEXFINDER...
Gastroenterology & Urology
7d
Cleared
Feb 14, 1997
FLEXFINDER GUIDEWIRE (REGULAR SHAFT/STIFF SHAFT) MARKED INK BANDS...
Gastroenterology & Urology
65d
Cleared
Aug 18, 1995
FINESSE GUIDEWIRE CORONARY
Cardiovascular
86d
Cleared
Jun 27, 1995
FLEXFINDER GUIDEWIRE
Cardiovascular
348d
Cleared
Jun 24, 1994
FLEXFINDER GUIDEWIRE
Gastroenterology & Urology
56d
Cleared
Jan 21, 1994
FLEXMEDICS SUPER-SEVEN STRANDED NICKEL-TITANIUM ARCHWIRE
Dental
143d
Cleared
Sep 24, 1991
FLEXMEDICS RETRACT ORTH PROBE, PETTINE BONE PROBE
Orthopedic
90d
Cleared
Apr 12, 1991
FLEXMEDICS MALLEABLE CANNULA
Orthopedic
56d
Cleared
May 23, 1990
FLEXMEDICS GUIDEWIRE .012 ONLY
Cardiovascular
229d
Cleared
Sep 26, 1989
FLEXMEDICS GUIDEWIRE
Cardiovascular
138d
Cleared
Jan 10, 1989
TIN COATED NITI ORTHODONTIC ARCH WIRES
Dental
32d
Cleared
Nov 14, 1988
FLEX PLASTIC PLASTIC COATED NITINOL ARCH WIRE
Dental
111d