Data / Medical devices / United States / Net Recovery Corp
Net Recovery Corp: FDA-registered device maker in Costa Mesa, CA, United States, 1 510(k) clearance
Net Recovery Corp is registered with the FDA (registration 3039168176) in Costa Mesa, CA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated May 29, 2024. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3039168176
- Address
- 650 Town Center Dr Ste 1590, Costa Mesa, CA, United States, 92626
- Owner or operator
- NET Recovery Corp (10093608)
- Roles
- Manufacturer
- First device listed
- June 11, 2025
- Registered through
- 2026
- Brand names listed
- NET Model 901, NET Model 902, NET Model 903
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Percutaneous Nerve Stimulator For Opioid Withdrawal | PZR | 2 | Manufacturer | 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 |
|---|---|---|---|---|---|---|
| May 29, 2024 | K233166 | NET Recovery Corp/NET Device | PZR | Substantially Equivalent | Net Recovery | accessdata.fda.gov |
Compare with other makers
Updated May 29, 2024. 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.