510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K854697Substantially Equivalent

Tubing Handpiece Replacement

Almore Intl., Inc., Portland OR / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K854697 is the FDA 510(k) clearance record for TUBING HANDPIECE REPLACEMENT, a class I device, cleared for Almore Intl., Inc. on under FDA product code EFB (Handpiece, Air-Powered, Dental). FDA records list 21 510(k) clearances for Almore Intl., Inc., from to . As of , FDA records show no recalls naming K854697.

Clearance record

Decision date
Received
(105 days to decision)
Product code
EFB Handpiece, Air-Powered, Dental
Regulation
21 CFR 872.4200
Device class
Class I
Review panel
Dental
Applicant
Almore Intl., Inc. Post Office Box 25214, Portland OR
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