Neal Dunning Assoc., Inc.
Country not established
- Devices
- 1
What Neal Dunning Assoc., Inc. makes
Neal Dunning Assoc., Inc. makes medical devices such as hot packs, including the RESTORE and THERMACELLS products.
The company's portfolio is regulated as Class I devices and is listed in the FDA 510(k) registry, with the company based in the US.
Catalogue
Restore, Thermacells (Hot Pack I) Ref K953442
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Neal Dunning Assoc., Inc. have in the registry?
The registry currently lists 1 device for Neal Dunning Assoc., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neal Dunning Assoc., Inc.'s devices?
Among its 1 most recently registered device, Neal Dunning Assoc., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Neal Dunning Assoc., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Neal Dunning Assoc., Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Neal Dunning Assoc., Inc. in the registry?
The most recently registered devices listed for Neal Dunning Assoc., Inc. include RESTORE, THERMACELLS (HOT PACK I).