Twin City Surgical, Inc.
United StatesFDA applicant, unverified
- Devices
- 6
What Twin City Surgical, Inc. makes
Twin City Surgical, Inc. manufactures surgical instruments for orthopedic and spinal procedures, including retractors, calipers, and specialized drivers for spinal fixation hardware. Their product line also includes a spinal wrench for adjusting implants, a CROM tester for assessing knee mobility, and a SIMS chair for intraoperative positioning.
The company’s devices are regulated under FDA Class I and Class II classifications, with most requiring 510(k) clearance. These instruments are listed in the FDA’s 510(k) database, and the manufacturer is based in the United States.
Catalogue
Sims Chair Ref K861632
Regimes: 510(k) Registry: 510(k)Spinal Wrench Ref K813067
Regimes: 510(k) Registry: 510(k)Anvil Retractor Ref K830585
Regimes: 510(k) Registry: 510(k)A Caliper Ref K820659
Regimes: 510(k) Registry: 510(k)The (Crom) Tester Ref K870767
Regimes: 510(k) Registry: 510(k)A Hook Driver Ref K820660
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Twin City Surgical, Inc. have in the registry?
The registry currently lists 6 devices for Twin City Surgical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Twin City Surgical, Inc.'s devices?
Among its 6 most recently registered devices, Twin City Surgical, Inc. has devices listed in FDA 510(k) (6 devices).
What risk classes do Twin City Surgical, Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Twin City 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 Twin City Surgical, Inc. in the registry?
The most recently registered devices listed for Twin City Surgical, Inc. include SIMS CHAIR, SPINAL WRENCH, ANVIL RETRACTOR and A CALIPER.