Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K252662Substantially Equivalent

UniBur

Nakanishi Inc., Kanuma, JP / Traditional, Substantially Equivalent

K252662 is the FDA 510(k) clearance record for UniBur, a class II device, cleared for Nakanishi, Inc. on under FDA product code HBE (Drills, Burrs, Trephines & Accessories (Simple, Powered)). FDA records list 40 510(k) clearances for Nakanishi, Inc., from to . As of , FDA records show no recalls naming K252662.

Clearance record

Decision date
Received
(28 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
Nakanishi, Inc. 700 Shimohinata, Kanuma, JP
510(k) summary
Summary PDF
Third party review
Yes

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