Data / Medical devices / United States / Arpwave LLC
Arpwave LLC: FDA-registered device maker in Apple Valley, MN, United States, 1 510(k) clearance
Arpwave LLC is registered with the FDA (registration 3004509773) in Apple Valley, MN, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated December 17, 2009. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3004509773
- Address
- 7721 145th Ave S, Apple Valley, MN, United States, 55124
- Owner or operator
- ARPwave LLC (10081917)
- Roles
- Repackager or relabeler
- First device listed
- May 26, 2021
- Registered through
- 2026
- Brand names listed
- Rx100, RxBlack
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Stimulator, Muscle, Powered | IPF | 2 | Repackager or relabeler | 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 |
|---|---|---|---|---|---|---|
| December 17, 2009 | K093259 | ARP RX100 | IPF | Substantially Equivalent | Arp Manufacturing, Inc. | accessdata.fda.gov |
Compare with other makers
Updated December 17, 2009. 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.