Pro Surgical, Inc.
United StatesFDA applicant, unverified FDA FEI 3031081659
- Devices
- 216
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Pro Surgical, Inc. makes
Pro Surgical, Inc. manufactures metallic spinal interbody fusion cages, reusable surgical instruments (including awls, drills, screwdrivers, and positioning tools), and orthopaedic counter-torque/rod-pushing instruments. Their portfolio includes the ProAM ALIF System, designed for anterior lumbar interbody fusion procedures. The company also provides reusable instrument trays for spinal and orthopaedic surgeries.
The company’s devices are regulated under FDA classifications, including Class I and Class II, with submissions recorded in the FDA’s 510(k) and UDI registries. The manufacturer is based in the United States.
Catalogue
Search and filter all 216 devicesShowing 1-50 of 216
Company details
- FDA FEI number
- 3031081659
- DUNS number
- 119149675
- Address
- 1910 Palomar Point Way, Suite 201, Carlsbad, CA, 92008
Frequently asked questions
How many devices does Pro Surgical, Inc. have in the registry?
The registry currently lists 216 devices for Pro Surgical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pro Surgical, Inc.'s devices?
Among its 50 most recently registered devices, Pro Surgical, Inc. has devices listed in FDA GUDID (50 devices).
What risk classes do Pro Surgical, Inc.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Pro Surgical, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pro Surgical, Inc. in the registry?
The most recently registered devices listed for Pro Surgical, Inc. include ProAM ALIF System LN-033425-1818, ProAM ALIF System LN-010401-0000-28, ProAM ALIF System LN-013425-0616 and ProAM ALIF System LN-033827-0616.