Inmark Corp.
United StatesFDA applicant, unverified
- Devices
- 4
What Inmark Corp. makes
Inmark Corp. manufactures X-ray tube housing assemblies, including the Polarix II GEN/XO 110 and Soredex DC/CIR 51 models. The company also provides services for the reloading of various X-ray tube housing assemblies.
These devices are classified as Class I medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Reloading Of X-Ray Tube Housing Assem., Various Ref K894742
Regimes: 510(k) Registry: 510(k)X-Ray Tube Housing Assembly Soredex Dc/Cir 51 Ref K910276
Regimes: 510(k) Registry: 510(k)X-Ray Tube Housing Assembly, Various Models Ref K894413
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Inmark Corp. have in the registry?
The registry currently lists 4 devices for Inmark Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Inmark Corp.'s devices?
Among its 4 most recently registered devices, Inmark Corp. has devices listed in FDA 510(k) (4 devices).
What risk classes do Inmark Corp.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Inmark Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Inmark Corp. in the registry?
The most recently registered devices listed for Inmark Corp. include X-RAY TUBE HOUSING ASSEMBLY POLARIX II GEN/XO 110, RELOADING OF X-RAY TUBE HOUSING ASSEM., VARIOUS, X-RAY TUBE HOUSING ASSEMBLY SOREDEX DC/CIR 51 and X-RAY TUBE HOUSING ASSEMBLY, VARIOUS MODELS.