Laser Photonics, Inc.
Orlando, FL, US
Laser Photonics, Inc. appears in FDA device records in Orlando, FL. FDA records list 14 510(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
- 14
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 14 510(k) clearances for Laser Photonics, Inc. between 1988 and 1994. The busiest year on record is 1990, with 5. The most recent is 1994, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1988 | 1 |
| 1990 | 5 |
| 1991 | 2 |
| 1992 | 2 |
| 1993 | 2 |
| 1994 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K934501 | LASER PHOTONICS ML755 DERMABLASER | GEX | Substantially Equivalent | |
| K933140 | RQM-1005 INTEGULASER RUBY MEDICAL LASER SYSTEM | GEX | Substantially Equivalent | |
| K924537 | LPI ML210 HOLMIUM SURGICAL LASER | GEX | Substantially Equivalent | |
| K920334 | LASERPHOTONICS ML300 STONELASER ALEXANDRITE LITH. | GEX | Substantially Equivalent | |
| K915631 | LPI ML 100/532 AND ML 532 SURGICAL LASER | GEX | Substantially Equivalent | |
| K914827 | LPI ML210 HOLMIUM SURGICAL LASER, MODIFICATION | GEX | Substantially Equivalent | |
| K904841 | LPI YAG MODEL 1003 SURGICAL LASER SYST/MODIFIED | GEX | Substantially Equivalent | |
| K910233 | LASER PHOTONICS ML-210 HOLMIUM:YAG MEDI LASE SYST | GEX | Substantially Equivalent | |
| K904354 | LPI MULILASE YAG/532 SURGICAL LASER SYSTEM | GEX | Substantially Equivalent | |
| K904331 | L.P.I. LASER DELIVERY SYSTEM | GEX | Substantially Equivalent | |
| K904229 | MULTILASE 60 | GEX | Substantially Equivalent | |
| K904227 | MULTILASE 45 | GEX | Substantially Equivalent | |
| K900837 | LPI YAG MODEL 1003 SURGICAL LASER SYSTEM | GEX | Substantially Equivalent | |
| K882738 | L.P.I. LASER DELIVERY SYSTEM | 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
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
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Data as of , FDA export datePage updated Source: openFDA, public domain
