Flexmedics
FDA 510(k) & PMA Approved Devices — 20 products
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Total Devices20
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K990765 | FLEXFINDER GUIDE WIRE(REGULAR SHAFT/STIFF SHAFT) MARKED INK BANDS, FLEXFINDER GUIDE WIRE (REGULAR SHAFT/STIFF SHAFT) NO | OCY | 1999-03-15 | View |
| 510(k) | K964955 | FLEXFINDER GUIDEWIRE (REGULAR SHAFT/STIFF SHAFT) MARKED INK BANDS ENCAP+/GUIDEWIRE(REGULAR SHAFT/STIFF SHAFT) NO MARKING | OCY | 1997-02-14 | View |
| 510(k) | K952430 | FINESSE GUIDEWIRE CORONARY | DQX | 1995-08-18 | View |
| 510(k) | K943390 | FLEXFINDER GUIDEWIRE | DQX | 1995-06-27 | View |
| 510(k) | K942074 | FLEXFINDER GUIDEWIRE | KNY | 1994-06-24 | View |
| 510(k) | K934265 | FLEXMEDICS SUPER-SEVEN STRANDED NICKEL-TITANIUM ARCHWIRE | DZC | 1994-01-21 | View |
| 510(k) | K912843 | FLEXMEDICS RETRACT ORTH PROBE, PETTINE BONE PROBE | HXB | 1991-09-24 | View |
| 510(k) | K910674 | FLEXMEDICS MALLEABLE CANNULA | HRX | 1991-04-12 | View |
| 510(k) | K895899 | FLEXMEDICS GUIDEWIRE .012 ONLY | DQX | 1990-05-23 | View |
| 510(k) | K893626 | FLEXMEDICS GUIDEWIRE | DQX | 1989-09-26 | View |
| 510(k) | K885086 | TIN COATED NITI ORTHODONTIC ARCH WIRES | EJF | 1989-01-10 | View |
| 510(k) | K883120 | FLEX PLASTIC PLASTIC COATED NITINOL ARCH WIRE | EJF | 1988-11-14 | View |
| 510(k) | K881331 | ORTHODONTIC NITINOL SPRINGS | EJW | 1988-04-21 | View |
| 510(k) | K881233 | STRAIGHT LENGTH ARCH WIRES | EJF | 1988-04-12 | View |
| 510(k) | K881274 | CENTER BEND ARCH WIRES | EJF | 1988-04-12 | View |
| 510(k) | K880882 | REVERSE CURVE ARCHWIRE | EJF | 1988-04-11 | View |
| 510(k) | K881163 | RECTANGULAR NITINOL ARCH WIRE | EJF | 1988-04-07 | View |
| 510(k) | K873649 | FLEX GOLD | EJF | 1987-10-05 | View |
| 510(k) | K870156 | FLEXMEDICS NITINOL MAMMORY WIRE | 1987-02-24 | View | |
| 510(k) | K863742 | FLEXMEDICS NITINOL ARCH WIRE | DZC | 1986-11-24 | View |
No matching devices.
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