510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K802243Substantially Equivalent

Vaxiom Family of RF Lesion Probes & Elec

Progress Mankind Technology, Hopkins MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K802243 is the FDA 510(k) clearance record for VAXIOM FAMILY OF RF LESION PROBES & ELEC, a class II device, cleared for Progress Mankind Technology on under FDA product code GXI (Probe, Radiofrequency Lesion). FDA records list 17 510(k) clearances for Progress Mankind Technology, from to . As of , FDA records show no recalls naming K802243.

Clearance record

Decision date
Received
(57 days to decision)
Product code
GXI Probe, Radiofrequency Lesion
Regulation
21 CFR 882.4725
Device class
Class II
Review panel
Neurology
Applicant
Progress Mankind Technology Box 464, Hopkins MN
Third party review
No

Clearances, product code GXI

Trailing 12 months
2 clearances under product code GXI in the twelve months to October 2026, February 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code GXI, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20261
March 20260
April 20261
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260