510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K801535Substantially Equivalent

Lares Handpiece Oil

Lares Manufacturing Co., Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K801535 is the FDA 510(k) clearance record for LARES HANDPIECE OIL, a class I device, cleared for Lares Manufacturing Co., Inc. on under FDA product code EFB (Handpiece, Air-Powered, Dental). FDA records list 6 510(k) clearances for Lares Manufacturing Co., Inc., from to . As of , FDA records show no recalls naming K801535.

Clearance record

Decision date
Received
(166 days to decision)
Product code
EFB Handpiece, Air-Powered, Dental
Regulation
21 CFR 872.4200
Device class
Class I
Review panel
Dental
Applicant
Lares Manufacturing Co., Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code EFB

Trailing 12 months
3 clearances under product code EFB in the twelve months to October 2026, January 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code EFB, trailing twelve months
MonthClearances
November 20250
December 20250
January 20262
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20261
October 20260