Home › Device types › PDZ
Lasers For Temporary Increase Of Clear Nail In Patients With Onychomycosis
FDA product code PDZ · Class 2 · General, Plastic Surgery
29
Registered devices
3
Adverse events
1
Recalls
19
510(k) clearances
Devices with this code
ZYE YAG — VYDENCE MEDICALZYE ALX — VYDENCE MEDICALGMAX Pro Laser System — Candela CorporationZYE-ULTRA FDA — VYDENCE MEDICALETHEREA-MX — VYDENCE MEDICALLightwalker DT ADVANCED — FOTONA d.o.o.Lightwalker DT — FOTONA d.o.o.Hyperblue plus — QUANTA SYSTEM SPAFotona XP-2 Focus — FOTONA d.o.o.Fotona XP Focus — FOTONA d.o.o.ONE FDA — VYDENCE MEDICALLightwalker ST-E ADVANCED — FOTONA d.o.o.Genesis Plus — CUTERA, INC.Lightwalker ST-E STAND — FOTONA d.o.o.SIRONA — Wuhan Dimed Laser Technology Co., Ltd.LongPulse — VYDENCE MEDICALLightForce EXPi — LITECURE LLCGIGAA — Gigaalaser Company Ltd.Genesis Plus 1 mm Spot Size Adapter — CUTERA, INC.LightForce EXP — LITECURE LLCFotona XP Focus — FOTONA d.o.o.Lightwalker ST-E — FOTONA d.o.o.5-15/lt — VYDENCE MEDICALREMY — Wuhan Dimed Laser Technology Co., Ltd.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2013-11-20 | Hyperion Medical | Brochures and web site information for the HyperBlue 1530 diode laser promoted features which had not been cleared in the product's premarket notification to th |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.
