Surgipros LLC
United Statesfrom the FDA registration address FDA establishment FEI 3012267976
- Devices
- 1,271
- Registrations
- FDA
- FDA recalls
- 0
What Surgipros LLC makes
SurgiPros LLC manufactures reusable surgical retractors, including blade systems and self-retaining frames, as well as spinal rongeurs and neurosurgical curettes designed for single-use. Their portfolio also includes vascular graft tunnellers, reusable soft-tissue manipulation forceps, and reusable suction cannulae for surgical and emergency procedures.
All devices fall under FDA Class I regulation and are listed in the FDA’s Unique Device Identification (UDI) system. The company operates from the United States.
Catalogue
Search and filter all 1,271 devicesShowing 1-50 of 1,271
Company details
- FDA FEI number
- 3012267976
- Address
- 4715 Arlington Rd., Palmetto, FL, 34221
Frequently asked questions
How many devices does SURGIPROS LLC have in the registry?
The registry currently lists 1271 devices for SURGIPROS LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list SURGIPROS LLC's devices?
Among its 50 most recently registered devices, SURGIPROS LLC has devices listed in FDA GUDID (50 devices).
What risk classes do SURGIPROS LLC's devices fall under?
Among its 50 most recently registered devices, the classes recorded for SURGIPROS LLC's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from SURGIPROS LLC in the registry?
The most recently registered devices listed for SURGIPROS LLC include SURGIPROS 010001SP, SurgiPros U-0186SP, SurgiPros U-0187SP and SurgiPros U-0189SP.