Light Age, Inc.
Somerset, NJ, US
Light Age, Inc. appears in FDA device records in Somerset, NJ. FDA records list 7 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 7
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 7 510(k) clearances for Light Age, Inc. between 1998 and 2012. The busiest year on record is 2004, with 2. The most recent is 2012, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1998 | 1 |
| 1999 | 1 |
| 2004 | 2 |
| 2009 | 1 |
| 2011 | 1 |
| 2012 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K113115 | EPICARE YAG | GEX | Substantially Equivalent | |
| K110370 | Q-CLEAR | PDZ | Substantially Equivalent | |
| K091625 | EPICARE-DUO LASER SYSTEM | GEX | Substantially Equivalent | |
| K032991 | LIGHT AGE EPICARE ALEXANDRITE LASER, MODELS 501-1H, 501-SP, 501-LP AND 501-LPX | GEX | Substantially Equivalent | |
| K033259 | LIGHT AGE Q-CLEAR LASER, MODEL 701-1101 | GEX | Substantially Equivalent | |
| K983977 | LIGHT AGE EPICARE ALEXANDRITE LASER | GEX | Substantially Equivalent | |
| K980131 | ALEX TA2 ERASER | GEX | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain