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Palomar Medical Products, Inc.

United StatesFDA applicant, unverified

Devices
21

What Palomar Medical Products, Inc. makes

Palomar Medical Products, Inc. makes laser and pulsed light systems, including the PALOMAR ASPIRE LASER PLATFORM, LIGHTSHEER LONG PULSE RUBY LASER, and PALOMAR STARLUX PULSED LIGHT SYSTEM, as well as handpieces and upgrade kits for these systems.

The company's portfolio is regulated as Class II devices and is listed in the FDA 510(k) registry, with the company based in the US.

AI-generated from registry data, 30 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue21

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  • Palomar Aspire Laser Platform Ref K081416

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Lightsheer Long Pulse Ruby Laser Ref K982980

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Palomar Aspire Laser Platform Ref K080567

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Palomar Starlux Pulsed Light System Ref K041086

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Modification To LUX1540 Handpiece And Lux 1440 Handpiece Ref K091446

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Erbium Fractional Handpiece Ref K083900

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Erbium Fractional Handpiece Ref K071768

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Palomar Aspire Laser Platform Ref K083165

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Palomar Lux 1540 Handpiece Ref K080244

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Modification To Palomar LUX1540 Handpiece Ref K073583

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Starlux Pulsed Light System Ref K033549

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Epilaser I Upgrade Kit Ref K980160

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Loi System Ref K090525

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Epilaser Normal Mode Ruby Laser Ref K980517

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Lightsheer Ref K980420

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Emerge Fractional Laser Ref K111840

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Thermapulse Ref K092222

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Palomar Erbium Handpiece Ref K071152

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Palomar LUX1540 Handpiece Ref K061652

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Palomar Lightcube Ref K024179

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Palomar Slp 1000 Ref K013028

    Active Regimes: 510(k) Registry: 510(k) Class:II

Rows 1-21 of 21

Frequently asked questions

How many devices does Palomar Medical Products, Inc. have in the registry?

The registry currently lists 21 devices for Palomar Medical Products, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Palomar Medical Products, Inc.'s devices?

Among its 21 most recently registered devices, Palomar Medical Products, Inc. has devices listed in FDA 510(k) (21 devices).

What risk classes do Palomar Medical Products, Inc.'s devices fall under?

Among its 21 most recently registered devices, the classes recorded for Palomar Medical Products, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Palomar Medical Products, Inc. in the registry?

The most recently registered devices listed for Palomar Medical Products, Inc. include PALOMAR ASPIRE LASER PLATFORM, LIGHTSHEER LONG PULSE RUBY LASER, PALOMAR STARLUX PULSED LIGHT SYSTEM and MODIFICATION TO LUX1540 HANDPIECE AND LUX 1440 HANDPIECE.

Generated automatically from registry data and not verified by a human reviewer.