510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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DEN980003Unknown

Diamond Probe/perio 2000 System

Diamond General Development Corp., Ann Arbor MI / Post-NSE, Unknown
FDA source (opens on fda.gov)

DEN980003 is the FDA 510(k) clearance record for DIAMOND PROBE/PERIO 2000 SYSTEM, a class II device, cleared for Diamond General Development Corp. on under FDA product code MVH (Device, Detection, Sulfide). FDA records list one 510(k) clearance for Diamond General Development Corp. As of , FDA records show no recalls naming DEN980003.

Clearance record

Decision date
Received
(60 days to decision)
Product code
MVH Device, Detection, Sulfide
Regulation
21 CFR 872.1870
Device class
Class II
Review panel
Dental
Applicant
Diamond General Development Corp. 333 Parkland Plz., Ann Arbor MI
Third party review
No

Clearances, product code MVH

Trailing 12 months

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

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