Light Age, Inc.
FDA 510(k) & PMA Approved Devices — 7 products
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Total Devices7
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K113115 | EPICARE YAG | GEX | 2012-04-03 | View |
| 510(k) | K110370 | Q-CLEAR | PDZ | 2011-09-15 | View |
| 510(k) | K091625 | EPICARE-DUO LASER SYSTEM | GEX | 2009-11-03 | View |
| 510(k) | K032991 | LIGHT AGE EPICARE ALEXANDRITE LASER, MODELS 501-1H, 501-SP, 501-LP AND 501-LPX | GEX | 2004-09-14 | View |
| 510(k) | K033259 | LIGHT AGE Q-CLEAR LASER, MODEL 701-1101 | GEX | 2004-02-25 | View |
| 510(k) | K983977 | LIGHT AGE EPICARE ALEXANDRITE LASER | GEX | 1999-01-07 | View |
| 510(k) | K980131 | ALEX TA2 ERASER | GEX | 1998-02-17 | View |
No matching devices.
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