Medicorp, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Medicorp, Inc. makes
Medicorp, Inc. manufactures concentrated dehydrated dialysate solutions for hemodialysis, including dehydrated dialysate concentrate, as well as devices for reprocessing dialyzers such as the ULTRAMAX III. Their portfolio also includes a negative pressure converter for medical applications and a portable traction device designed for orthopedic use.
The company’s products are regulated under the FDA’s 510(k) pathway, with devices classified as either Class I or Class II. These products are listed in the FDA’s 510(k) database, and the company is headquartered in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Ultramax Iii, Dialyzer Reprocessing Device Ref K860026
Regimes: 510(k) Registry: 510(k)Negatove Pressure Convertor Ref K791164
Regimes: 510(k) Registry: 510(k)Medi-Trak Portable Traction Device Ref K791396
Regimes: 510(k) Registry: 510(k)Ultramax Ref K832705
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medicorp, Inc. have in the registry?
The registry currently lists 5 devices for Medicorp, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medicorp, Inc.'s devices?
Among its 5 most recently registered devices, Medicorp, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Medicorp, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Medicorp, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medicorp, Inc. in the registry?
The most recently registered devices listed for Medicorp, Inc. include MEDICORP DEHYDRACON A DEHYDRATED DIALYSATE CONCENT, ULTRAMAX III, DIALYZER REPROCESSING DEVICE, NEGATOVE PRESSURE CONVERTOR and MEDI-TRAK PORTABLE TRACTION DEVICE.