510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K813328Substantially Equivalent

Myerson/kenson Gp Polymer

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

K813328 is the FDA 510(k) clearance record for MYERSON/KENSON GP POLYMER, a class II device, cleared for Howmedica Corp. on under FDA product code EBD (Coating, Filling Material, Resin). FDA records list 409 510(k) clearances for Howmedica Corp., from to . As of , FDA records show no recalls naming K813328.

Clearance record

Decision date
Received
(92 days to decision)
Product code
EBD Coating, Filling Material, Resin
Regulation
21 CFR 872.3310
Device class
Class II
Review panel
Dental
Applicant
Howmedica Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code EBD

Trailing 12 months
1 clearance under product code EBD in the twelve months to October 2026, April 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code EBD, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20261
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260