510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K883922Substantially Equivalent

Techmedica I.b.o. Blade

Techmedica, Inc., Camarillo CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K883922 is the FDA 510(k) clearance record for TECHMEDICA I.B.O. BLADE, a class II device, cleared for Techmedica, Inc. on under FDA product code DZJ (Driver, Wire, And Bone Drill, Manual). FDA records list 31 510(k) clearances for Techmedica, Inc., from to . As of , FDA records show no recalls naming K883922.

Clearance record

Decision date
Received
(83 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
Techmedica, Inc. 1380 Flynn Rd., Camarillo CA
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