U.S. Medical Instruments, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What U.S. Medical Instruments, Inc. makes
U.S. Medical Instruments, Inc. manufactures safety syringes designed to reduce needle-stick injuries during medical procedures, including the SAFETYSNAP and SAFESNAP models.
These devices are classified as Class II under U.S. regulations and are listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Safetysnap Safety Syringe Ref K910520
510(k) 510(k)Safesnap Safety Syringe Ref K925039
510(k) 510(k)
Frequently asked questions
How many devices does U.S. Medical Instruments, Inc. have in the registry?
The registry currently lists 2 devices for U.S. Medical Instruments, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list U.S. Medical Instruments, Inc.'s devices?
Among its 2 most recently registered devices, U.S. Medical Instruments, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do U.S. Medical Instruments, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for U.S. Medical Instruments, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from U.S. Medical Instruments, Inc. in the registry?
The most recently registered devices listed for U.S. Medical Instruments, Inc. include SAFETYSNAP SAFETY SYRINGE and SAFESNAP SAFETY SYRINGE.