510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K170423Substantially Equivalent

DentureID Microchip

Cmp Industries, LLC, Albany NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K170423 is the FDA 510(k) clearance record for DentureID Microchip, a class II device, cleared for Cmp Industries, LLC on under FDA product code PYQ (Rfid Chip For Dental Appliance). FDA's definition for product code PYQ reads: "The device is intended to enable access to secure patient identification and device information when used with complete dentures, partial dentures, and other removable oral appliances". FDA records list 7 510(k) clearances for Cmp Industries, LLC, from to . As of , FDA records show no recalls naming K170423.

Clearance record

Decision date
Received
(254 days to decision)
Product code
PYQ Rfid Chip For Dental Appliance
Regulation
21 CFR 880.6300
Device class
Class II
Review panel
General Hospital
Applicant
Cmp Industries, LLC 413 N. Pearl St., Albany NY
510(k) summary
Summary PDF
Third party review
No

Clearances, product code PYQ

Trailing 12 months

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

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