KLS-Martin L.P.
United Statesfrom the FDA registration address FDA FEI 1000525271
- Devices
- 14,248
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What KLS-Martin L.P. makes
KLS-Martin L.P. manufactures reusable surgical instruments, including craniofacial fixation plates and screws (non-bioabsorbable), implantable craniofacial bone distractors, spinal rongeurs, soft-tissue manipulation forceps, and hand-held retractors. Their portfolio also includes orthopaedic bone screws (non-sliding) and general-purpose surgical scissors.
The company’s devices are regulated under FDA’s Class I and Class II classifications and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in the United States.
Catalogue
Search and filter all 14,248 devicesShowing 1-50 of 14,248
Company details
- FDA FEI number
- 1000525271
- DUNS number
- 826499238
- Address
- 11201 Saint Johns Industrial Pkwy S, Jacksonville, FL, 32246
- [email protected]
- Phone
- +1(904)641-7746
Frequently asked questions
How many devices does KLS-Martin L.P. have in the registry?
The registry currently lists 14248 devices for KLS-Martin L.P.. Devices recorded under merged duplicate company entries are counted once.
Which registries list KLS-Martin L.P.'s devices?
Among its 50 most recently registered devices, KLS-Martin L.P. has devices listed in FDA GUDID (50 devices).
What risk classes do KLS-Martin L.P.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for KLS-Martin L.P.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from KLS-Martin L.P. in the registry?
The most recently registered devices listed for KLS-Martin L.P. include LEVEL ONE CMF, STERILE 50-280-00-71, LEVEL ONE CMF, STERILE 50-280-03-71, LEVEL ONE CMF, STERILE 50-280-05-71 and LEVEL ONE CMF, STERILE 50-280-07-71.