Data / Medical devices / United States / Pepper Interactive Inc
Pepper Interactive Inc: FDA-registered device maker in Wilmington, DE, United States, 1 510(k) clearance
Pepper Interactive Inc is registered with the FDA (registration 3044675848) in Wilmington, DE, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated January 16, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3044675848
- Address
- 251 Little Falls Dr, Wilmington, DE, United States, 19808
- Owner or operator
- Pepper Interactive Inc (10095704)
- Roles
- Specification developer
- First device listed
- April 16, 2026
- Registered through
- 2026
- Brand names listed
- Pepper EMS Suit, Pepper EMS Training System, Pepper Muscle Activation Suit
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Stimulator, Muscle, Powered, For Muscle Conditioning | NGX | 2 | Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| January 16, 2025 | K233770 | Pepper EMS Training System | NGX | Substantially Equivalent | Pepper Interactive, Inc. | accessdata.fda.gov |
Compare with other makers
Updated January 16, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.