510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K880179Substantially Equivalent

Beavers' Dental Diamond Instruments

Beavers Dental, Div. Sybron Canada, Ltd., Washington DC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K880179 is the FDA 510(k) clearance record for BEAVERS' DENTAL DIAMOND INSTRUMENTS, a class I device, cleared for Beavers Dental, Div. Sybron Canada, Ltd. on under FDA product code DZP (Instrument, Diamond, Dental). FDA records list 3 510(k) clearances for Beavers Dental, Div. Sybron Canada, Ltd., from to . As of , FDA records show no recalls naming K880179.

Clearance record

Decision date
Received
(56 days to decision)
Product code
DZP Instrument, Diamond, Dental
Regulation
21 CFR 872.4535
Device class
Class I
Review panel
Dental
Applicant
Beavers Dental, Div. Sybron Canada, Ltd. One Thomas Cir., Washington DC
Third party review
No

Clearances, product code DZP

Trailing 12 months

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

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