510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K861502Substantially Equivalent

Eoh 8501 Osseointegrated Implant System

Dr. Harold Bergman, Canada, CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K861502 is the FDA 510(k) clearance record for EOH 8501 OSSEOINTEGRATED IMPLANT SYSTEM, a class II device, cleared for Dr. Harold Bergman on under FDA product code DZE (Implant, Endosseous, Root-Form). FDA records list one 510(k) clearance for Dr. Harold Bergman. As of , FDA records show no recalls naming K861502.

Clearance record

Decision date
Received
(64 days to decision)
Product code
DZE Implant, Endosseous, Root-Form
Regulation
21 CFR 872.3640
Device class
Class II
Review panel
Dental
Applicant
Dr. Harold Bergman #200 - 805 W. Broadway, 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