Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K894151Substantially Equivalent

Irrigated Drill for Ss Submerged Screw Plant

Artech Corp., Chantilly VA / Traditional, Substantially Equivalent

K894151 is the FDA 510(k) clearance record for IRRIGATED DRILL FOR SS SUBMERGED SCREW PLANT, a class II device, cleared for Artech Corp. on under FDA product code DZJ (Driver, Wire, And Bone Drill, Manual). FDA records list 8 510(k) clearances for Artech Corp., from to . As of , FDA records show no recalls naming K894151.

Clearance record

Decision date
Received
(105 days to decision)
Product code
DZJ Driver, Wire, And Bone Drill, Manual
Regulation
21 CFR 872.4120
Device class
Class II
Review panel
Dental
Applicant
Artech Corp. 14554 Lee Rd., Chantilly VA
Third party review
No

Clearances, product code DZJ

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