Transcorp, Inc.
United StatesFDA applicant, unverified
- Devices
- 10
What Transcorp, Inc. makes
Transcorp, Inc. makes spinal fixation and access systems, including the ACIF system, Trans-Plate anterior cervical plate system, and Spinal Access system.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Steriletx Powder Free Latex Examination Gloves Ref K915189
Regimes: 510(k) Registry: 510(k)Latex Examination Gloves Ref K922439
Regimes: 510(k) Registry: 510(k)Transcorp Acif System Ref K092794
Regimes: 510(k) Registry: 510(k)Sri Johani Latex Surgeons Gloves Ref K904662
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Transcorp Spinal Access System Ref K113352
Regimes: 510(k) Registry: 510(k)Kleartex Latex Surgical Gloves Ref K903069
Regimes: 510(k) Registry: 510(k)Medpride Latex Examination Gloves Ref K894569
Regimes: 510(k) Registry: 510(k)Texmed Latex Examination Glove Ref K891120
Regimes: 510(k) Registry: 510(k)Transcorp Acif System Ref K121178
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Transcorp, Inc. have in the registry?
The registry currently lists 10 devices for Transcorp, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Transcorp, Inc.'s devices?
Among its 10 most recently registered devices, Transcorp, Inc. has devices listed in FDA 510(k) (10 devices).
What risk classes do Transcorp, Inc.'s devices fall under?
Among its 10 most recently registered devices, the classes recorded for Transcorp, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Transcorp, Inc. in the registry?
The most recently registered devices listed for Transcorp, Inc. include STERILETX POWDER FREE LATEX EXAMINATION GLOVES, LATEX EXAMINATION GLOVES, TRANSCORP ACIF SYSTEM and SRI JOHANI LATEX SURGEONS GLOVES.