510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K892255Substantially Equivalent

Dental Root Elevator

Zinnanti Surgical Instruments, Inc., Chatsworth CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K892255 is the FDA 510(k) clearance record for DENTAL ROOT ELEVATOR, a class II device, cleared for Zinnanti Surgical Instruments, Inc. on under FDA product code EKO (Denture Preformed (Partially Prefabricated Denture)). FDA records list 76 510(k) clearances for Zinnanti Surgical Instruments, Inc., from to . As of , FDA records show no recalls naming K892255.

Clearance record

Decision date
Received
(27 days to decision)
Product code
EKO Denture Preformed (Partially Prefabricated Denture)
Regulation
21 CFR 872.3600
Device class
Class II
Review panel
Dental
Applicant
Zinnanti Surgical Instruments, Inc. 21540-B Prairie St., Chatsworth CA
Third party review
No

Clearances, product code EKO

Trailing 12 months

FDA records hold no clearances under product code EKO in the trailing twelve months.

FDA records show no clearances under product code EKO in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code EKO, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260