510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K820685Substantially Equivalent

Denture Adjustment Kit

Camdent Laboratories, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K820685 is the FDA 510(k) clearance record for DENTURE ADJUSTMENT KIT, a class II device, cleared for Camdent Laboratories on under FDA product code EBO (Denture Repair Kit). FDA's definition for product code EBO reads: "This product code has been established in accordance with the may 20, 1997, guidance entitled, convenience kits interim regulatory guidance, found at www.Fda.Gov/cdrh/ode/convkit.Html. This type of convenience kit, as listed in the...". FDA records list one 510(k) clearance for Camdent Laboratories. As of , FDA records show no recalls naming K820685.

Clearance record

Decision date
Received
(29 days to decision)
Product code
EBO Denture Repair Kit
Regulation
21 CFR 872.3570
Device class
Class II
Review panel
Dental
Applicant
Camdent Laboratories 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code EBO

Trailing 12 months

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

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