SpineNet LLC
United Statesfrom the FDA registration address FDA establishment FEI 3006755626
- Devices
- 53
- Registrations
- FDA
- FDA recalls
- 2
Catalogue
Search and filter all 53 devicesShowing 1-50 of 53
Company details
- FDA FEI number
- 3006755626
- Address
- 901 N. Lake Destiny Rd, Maitland, FL, 32751
FDA recalls
2013
- 5 Feb 2013 Z-2103-2013 Class II Terminated The recall decision has been made because because it has recently been determined that the instructions for use (IFU) had certain statements that should have been removed prior to initial product marketing.
- 4 Feb 2013 Z-2107-2013 Class II Terminated SpineNet was marketing this device to be used with SpineNet ACC device without FDA clearance or approval.
Frequently asked questions
How many devices does SpineNet LLC have in the registry?
The registry currently lists 53 devices for SpineNet LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list SpineNet LLC's devices?
Among its 50 most recently registered devices, SpineNet LLC has devices listed in FDA GUDID (50 devices).
What risk classes do SpineNet LLC's devices fall under?
Among its 50 most recently registered devices, the classes recorded for SpineNet LLC's devices are Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for SpineNet LLC?
FDA recall records list 2 recalls initiated by SpineNet LLC, the most recent initiated on 2013-02-05. 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 SpineNet LLC in the registry?
The most recently registered devices listed for SpineNet LLC include SPINENET ACC ® CGRP1300, SpineNet SSP® SSP® Fixed Screw, SPINENET ACC® CTL101207 and SPINENET ACC® CL121410.