Levitronix, LLC
United StatesFDA applicant, unverified
- Devices
- 11
- FDA recalls
- 2
At a glance
Market reach
- United States
- FDA recalls
Catalogue
Search and filter all 11 devicesFDA recalls
2008
- 17 Mar 2008 Z-1901-2008 Unclassified (pre-2012) Terminated Stops pumping: Interruption of CentriMag System support may occur when using a Valleylab Force FX-C Electrocautery Unit
Full distribution text
- 17 Mar 2008 Z-1902-2008 Unclassified (pre-2012) Terminated Stops pumping: Interruption of CentriMag System support may occur when using a Valleylab Force FX-C Electrocautery Unit
Full distribution text
- 17 Mar 2008 Z-1901-2008 Unclassified (pre-2012) Terminated Stops pumping: Interruption of CentriMag System support may occur when using a Valleylab Force FX-C Electrocautery Unit
Frequently asked questions
How many devices does Levitronix, LLC have in the registry?
The registry currently lists 11 devices for Levitronix, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Levitronix, LLC's devices?
Among its 11 most recently registered devices, Levitronix, LLC has devices listed in FDA 510(k) (11 devices).
What risk classes do Levitronix, LLC's devices fall under?
Among its 11 most recently registered devices, the classes recorded for Levitronix, LLC's devices are Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for Levitronix, LLC?
FDA recall records list 2 recalls initiated by Levitronix, LLC, the most recent initiated on 17 Mar 2008. 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 Levitronix, LLC in the registry?
The most recently registered devices listed for Levitronix, LLC include LEVITRONIX CENTRIMAG PRIMARY CONSOLE, LEVITRONIX CENTRIMAG PRIMARY AND BACKUP CONSOLES, CENTRIMAG DRAINAGE CANNULA KIT and LEVITRONIX 2ND GENERATION CENTRIMAG PRIMARY CONSOLE, LEVITRONIX MONITOR.