510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K972019Substantially Equivalent

Pefect Shot

International Imaging Electronics, Bolingbrook IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K972019 is the FDA 510(k) clearance record for PEFECT SHOT, a class I device, cleared for International Imaging Electronics on under FDA product code EIA (Unit, Operative Dental). FDA records list 19 510(k) clearances for International Imaging Electronics, from to . As of , FDA records show no recalls naming K972019.

Clearance record

Decision date
Received
(32 days to decision)
Product code
EIA Unit, Operative Dental
Regulation
21 CFR 872.6640
Device class
Class I
Review panel
Dental
Applicant
International Imaging Electronics 881 Remington Blvd., Bolingbrook IL
510(k) summary
Statement
Third party review
No

Clearances, product code EIA

Trailing 12 months
2 clearances under product code EIA 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 EIA, trailing twelve months
MonthClearances
November 20251
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20261
September 20260
October 20260