510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K233166Substantially Equivalent

NET Recovery Corp/NET Device

Net Recovery Corp, Anaheim Hills CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K233166 is the FDA 510(k) clearance record for NET Recovery Corp/NET Device, a class II device, cleared for Net Recovery on under FDA product code PZR (Percutaneous Nerve Stimulator For Opioid Withdrawal). FDA's definition for product code PZR reads: "Stimulate nerve branches to aid in the reduction of symptoms associated with substance use disorders". FDA records list one 510(k) clearance for Net Recovery. As of , FDA records show no recalls naming K233166.

Clearance record

Decision date
Received
(245 days to decision)
Product code
PZR Percutaneous Nerve Stimulator For Opioid Withdrawal
Regulation
21 CFR 882.5896
Device class
Class II
Review panel
Neurology
Applicant
Net Recovery 155 N Riverview Dr., Anaheim Hills CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code PZR

Trailing 12 months

FDA records hold no clearances under product code PZR in the trailing twelve months.

FDA records show no clearances under product code PZR in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code PZR, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260