510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K881924Substantially Equivalent

Endosseous Dental Implant

Bone Anchorage Systems, Inc., Toronto, Canada, CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K881924 is the FDA 510(k) clearance record for ENDOSSEOUS DENTAL IMPLANT, a class II device, cleared for Bone Anchorage Systems, Inc. on under FDA product code DZE (Implant, Endosseous, Root-Form). FDA records list one 510(k) clearance for Bone Anchorage Systems, Inc. As of , FDA records show no recalls naming K881924.

Clearance record

Decision date
Received
(35 days to decision)
Product code
DZE Implant, Endosseous, Root-Form
Regulation
21 CFR 872.3640
Device class
Class II
Review panel
Dental
Applicant
Bone Anchorage Systems, Inc. 298 Kennedy Ave., Toronto, Canada, CA
Third party review
No

Clearances, product code DZE

Trailing 12 months
19 clearances under product code DZE in the twelve months to October 2026, December 2025 the highest month at 4.
Show the numbers
Monthly 510(k) clearances under FDA product code DZE, trailing twelve months
MonthClearances
November 20251
December 20254
January 20261
February 20262
March 20264
April 20260
May 20261
June 20264
July 20260
August 20261
September 20261
October 20260