Reed Products, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Reed Products, Inc. makes
Reed Products, Inc. manufactures first-aid emergency medical systems and specialized trauma kits, including solutions for bone injuries, eye injuries, and burns. These products are designed for immediate on-site medical response in non-clinical settings, such as workplaces and public spaces.
The company’s products are regulated under FDA Class I and Class II (N) classifications, with most devices listed via the 510(k) pathway. They are based in the United States and appear in the FDA’s 510(k) registry.
Catalogue
First Response Emerg. Medical System Ref K841897
Regimes: 510(k) Registry: 510(k)First Response Emerg. Medical Sys Bones Ref K841899
Regimes: 510(k) Registry: 510(k)First Response Emerg. Eye Injuries Ref K841900
Regimes: 510(k) Registry: 510(k)First Response Emerg. Medicsl - Burns Ref K841898
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Reed Products, Inc. have in the registry?
The registry currently lists 4 devices for Reed Products, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Reed Products, Inc.'s devices?
Among its 4 most recently registered devices, Reed Products, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Reed Products, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Reed Products, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Reed Products, Inc. in the registry?
The most recently registered devices listed for Reed Products, Inc. include FIRST RESPONSE EMERG. MEDICAL SYSTEM, FIRST RESPONSE EMERG. MEDICAL SYS BONES, FIRST RESPONSE EMERG. EYE INJURIES and FIRST RESPONSE EMERG. MEDICSL - BURNS.