NET RECOVERY CORP

FDA Device Registration & Listing · Costa Mesa, CA, US · Registration 3039168176

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3039168176
FEI Number
3039168176
Entity Name
NET RECOVERY CORP
City/State/Country
Costa Mesa, CA, US
Establishment Address
650 Town Center Dr Ste 1590, Costa Mesa, CA 92626, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
NET Recovery Corp (Owner Number: 10093608)
Owner / Operator Contact Address
NET Recovery Corp, PO Box 849, Wilmington, DE 19899, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K233166
PMA Number
N/A

All Registered Proprietary Names

NET Model 903 NET Model 902 NET Model 901

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PZR Percutaneous Nerve Stimulator For Opioid Withdrawal Neurology Class 2 882.5896 2025-06-11

Official Correspondent

Eric Moyer

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

NET Recovery Corp
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3039168176. Last updated year: 2026. Please use registration number 3039168176 when referencing this establishment in official correspondence.
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