U.S. Mfg. & Management, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 5
What U.S. Mfg. & Management, Inc. makes
U.S. Mfg. & Management, Inc. produces passive motion therapy devices, including controlled passive motion machines for joint rehabilitation, as well as intravenous (IV) access kits designed for pediatric, geriatric, and general use. Their portfolio also includes fluid sampling packs for medical specimen collection and specialized IV restart kits for re-establishing venous access.
All listed devices fall under Class I regulatory classification in the U.S., with authorisation via 510(k) clearance through the FDA. The company operates within the United States.
Catalogue
Controlled Passive Motion Machine Ref K920860
510(k) 510(k)Veni-Shield Ref K842999
510(k) 510(k)Modified I.V. Start, Re-Start, Pedi And Geri-Kit Ref K862335
510(k) 510(k)- 510(k) 510(k)
Fluid Sampling Pack Ref K874436
510(k) 510(k)
Frequently asked questions
How many devices does U.S. Mfg. & Management, Inc. have in the registry?
The registry currently lists 5 devices for U.S. Mfg. & Management, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list U.S. Mfg. & Management, Inc.'s devices?
Among its 5 most recently registered devices, U.S. Mfg. & Management, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do U.S. Mfg. & Management, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for U.S. Mfg. & Management, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from U.S. Mfg. & Management, Inc. in the registry?
The most recently registered devices listed for U.S. Mfg. & Management, Inc. include CONTROLLED PASSIVE MOTION MACHINE, VENI-SHIELD, MODIFIED I.V. START, RE-START, PEDI AND GERI-KIT and I.V. START KIT, I.V. RESTART KIT, PEDI-KIT, GERI-KI.