Amd Lasers, LLC
United StatesFDA applicant, unverified
- Devices
- 20
- FDA recalls
- 1
At a glance
Market reach
- United States
- FDA recalls
Catalogue
Search and filter all 20 devicesFDA recalls
2010
- 15 Apr 2010 Z-2349-2010 Unclassified (pre-2012) Terminated Product is noncompliant with the Federal laser product performance standard in certain requirements. The ON/OFF key on some of the Picasso/Picasso Lite lasers could be removed with force while the key was in the ON position.
Frequently asked questions
How many devices does Amd Lasers, LLC have in the registry?
The registry currently lists 20 devices for Amd Lasers, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Amd Lasers, LLC's devices?
Among its 20 most recently registered devices, Amd Lasers, LLC has devices listed in FDA 510(k) (2 devices) and FDA GUDID (18 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Amd Lasers, LLC's devices fall under?
Among its 20 most recently registered devices, the classes recorded for Amd Lasers, LLC's devices are Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for Amd Lasers, LLC?
FDA recall records list 1 recall initiated by Amd Lasers, LLC, the most recent initiated on 15 Apr 2010. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.
What are the newest devices from Amd Lasers, LLC in the registry?
The most recently registered devices listed for Amd Lasers, LLC include Quadra Tip QT, Multi-Tip Handpiece - Picasso Lite Plus (Black) MTHP-PLPLUS, 400um Strippable Fiber - Plus Series SF400-PLUS and Picasso Plus Dental Diode Laser P810.