Pepper Interactive, Inc.
United Statesfrom the FDA registration address FDA FEI 3044675848
- Devices
- 12
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Pepper Interactive, Inc. makes
Pepper Interactive, Inc. manufactures the Pepper EMS Training System, which is a medical device used for emergency medical services training.
The Pepper EMS Training System is classified as a Class II medical device and is listed in the FDA 510(k) registry. Pepper Interactive, Inc. is based in the US.
Catalogue
Search and filter all 12 devicesCompany details
- FDA FEI number
- 3044675848
- DUNS number
- 118381742
- Address
- 251 Little Falls Dr, Wilmington, DE, 19808
Frequently asked questions
How many devices does Pepper Interactive, Inc. have in the registry?
The registry currently lists 12 devices for Pepper Interactive, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pepper Interactive, Inc.'s devices?
Among its 12 most recently registered devices, Pepper Interactive, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (11 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Pepper Interactive, Inc.'s devices fall under?
Among its 12 most recently registered devices, the classes recorded for Pepper Interactive, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pepper Interactive, Inc. in the registry?
The most recently registered devices listed for Pepper Interactive, Inc. include PEPPER Power Box, PEPPER EMS Suit and Pepper EMS Training System.