Lanx, Inc.
United StatesFDA applicant, unverified
- Devices
- 36
- FDA recalls
- 1
At a glance
Market reach
- United States
- FDA recalls
Catalogue
Search and filter all 36 devicesFDA recalls
2013
- 4 Nov 2013 Z-0400-2014 Class II Terminated Lanx, Inc. is recalling various lots of Timberline MPF Straight Split Tip Driver - Short ("Driver") because the width of the most distal end from the Driver handle (the tip of the hex portion of the Driver) is oversized.
Frequently asked questions
How many devices does Lanx, Inc. have in the registry?
The registry currently lists 36 devices for Lanx, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lanx, Inc.'s devices?
Among its 36 most recently registered devices, Lanx, Inc. has devices listed in FDA 510(k) (36 devices).
What risk classes do Lanx, Inc.'s devices fall under?
Among its 36 most recently registered devices, the classes recorded for Lanx, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for Lanx, Inc.?
FDA recall records list 1 recall initiated by Lanx, Inc., the most recent initiated on 4 Nov 2013. 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 Lanx, Inc. in the registry?
The most recently registered devices listed for Lanx, Inc. include LANX SPINAL FIXATION SYSTEM, MODIFICATION TO LANX POSTERIOR CERVICOTHORACIC SPINAL FIXATION SYSTEM, LANX CERVICAL INTERVERTEBRAL BODY FUSION SYSTEM and LANX ANTERIOR CERVIAL PLATE SYSTEM.