510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K875224Substantially Equivalent

Hudson Craninal Burrs

Tri-Med, Inc., Warsaw IN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K875224 is the FDA 510(k) clearance record for HUDSON CRANINAL BURRS, a class II device, cleared for Tri-Med, Inc. on under FDA product code HBE (Drills, Burrs, Trephines & Accessories (Simple, Powered)). FDA records list 29 510(k) clearances for Tri-Med, Inc., from to . As of , FDA records show no recalls naming K875224.

Clearance record

Decision date
Received
(37 days to decision)
Product code
HBE Drills, Burrs, Trephines & Accessories (Simple, Powered)
Regulation
21 CFR 882.4310
Device class
Class II
Review panel
Neurology
Applicant
Tri-Med, Inc. P.O. Box 701, Warsaw IN
Third party review
No

Clearances, product code HBE

Trailing 12 months
2 clearances under product code HBE in the twelve months to October 2026, November 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code HBE, trailing twelve months
MonthClearances
November 20251
December 20250
January 20260
February 20260
March 20261
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260