Data / Medical devices / United States / Laser Dental Innovations

Laser Dental Innovations: FDA-registered device maker in San Jose, CA, United States, 1 510(k) clearance

Laser Dental Innovations is registered with the FDA (registration 3003610527) in San Jose, CA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated January 18, 2000. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number

3003610527

Address

1219 Quail Creek Cir, San Jose, CA, United States, 95120

Owner or operator

LASER DENTAL INNOVATIONS (9039323)

Roles

Manufacturer

First device listed

November 14, 2007

Registered through

2026

Brand names listed

Litesaber Handpiece and tip, Starlite Fiber

Devices it lists

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.

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Updated January 18, 2000. 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.