510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K973800Substantially Equivalent

23:1 Reduction Angle

Midwest Dental Products Corp., Des Plaines IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K973800 is the FDA 510(k) clearance record for 23:1 REDUCTION ANGLE, a class I device, cleared for Midwest Dental Products Corp. on under FDA product code EGS (Handpiece, Contra- And Right-Angle Attachment, Dental). FDA records list 5 510(k) clearances for Midwest Dental Products Corp., from to . As of , FDA records show no recalls naming K973800.

Clearance record

Decision date
Received
(156 days to decision)
Product code
EGS Handpiece, Contra- And Right-Angle Attachment, Dental
Regulation
21 CFR 872.4200
Device class
Class I
Review panel
Dental
Applicant
Midwest Dental Products Corp. 901 W. Oakton St., Des Plaines IL
510(k) summary
Statement
Third party review
No

Clearances, product code EGS

Trailing 12 months

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

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