Data / Medical devices / Italy / Lasering S.R.L.
Lasering S.R.L.: FDA-registered device maker in MODENA Emilia-Romagna, Italy, 3 510(k) clearances
Lasering S.R.L. is registered with the FDA (registration 3004710757) in MODENA Emilia-Romagna, Italy. It lists 2 device types. The FDA files 3 510(k) clearances under its listings, the newest dated July 22, 2011. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3004710757
- Address
- Via Staffette Partigiane,54, MODENA Emilia-Romagna, Italy, 41122
- Owner or operator
- LASERING S.R.L. (9042050)
- Roles
- Exporter to the US, Manufacturer
- First device listed
- April 25, 2006
- Registered through
- 2027
- Brand names listed
- MULTIPLE SURGICAL A, Multiple Surgical A
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Powered Laser Surgical Instrument | GEX | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Powered Laser Surgical Instrument With MicrobeamFractional Output | ONG | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| July 22, 2011 | K110984 | SLIM E30 II CO2 LASER | ONG | Substantially Equivalent | Lasering S.R.L. | accessdata.fda.gov |
| March 7, 2007 | K063001 | SLIM EVOLUTION FAMILY OF CO2 LASERS AND DELIVERY DEVICE ACCESSORIES | GEX | Substantially Equivalent | Lasering S.R.L. | accessdata.fda.gov |
| January 17, 2007 | K063396 | VELURE FAMILY OF DIODE LASERS AND DELIVERY DEVICE ACCESSORIES | GEX | Substantially Equivalent | Lasering S.R.L. | accessdata.fda.gov |
Compare with other makers
- All makers of Powered Laser Surgical Instrument
- All makers of Powered Laser Surgical Instrument With MicrobeamFractional Output
Updated July 22, 2011. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.