510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K973248Substantially Equivalent

Imtec Bone Collector System

Imtec Corp., Ardmore OK / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K973248 is the FDA 510(k) clearance record for IMTEC BONE COLLECTOR SYSTEM, a class I device, cleared for Imtec Corp. on under FDA product code EHZ (Evacuator, Oral Cavity). FDA records list 26 510(k) clearances for Imtec Corp., from to . As of , FDA records show no recalls naming K973248.

Clearance record

Decision date
Received
(82 days to decision)
Product code
EHZ Evacuator, Oral Cavity
Regulation
21 CFR 872.6640
Device class
Class I
Review panel
Dental
Applicant
Imtec Corp. 2401 N. Commerce, Ardmore OK
510(k) summary
Summary
Third party review
No

Clearances, product code EHZ

Trailing 12 months

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

FDA records show no clearances under product code EHZ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code EHZ, 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