510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K830667Substantially Equivalent

Silicone-Silver Penile Prosthesis-Esk

Dacomed Corp., Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K830667 is the FDA 510(k) clearance record for SILICONE-SILVER PENILE PROSTHESIS-ESK, a class II device, cleared for Dacomed Corp. on under FDA product code FTQ (Prosthesis, Penis, Rigid Rod). FDA records list 20 510(k) clearances for Dacomed Corp., from to . As of , FDA records show no recalls naming K830667.

Clearance record

Decision date
Received
(230 days to decision)
Product code
FTQ Prosthesis, Penis, Rigid Rod
Regulation
21 CFR 876.3630
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Dacomed Corp. 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code FTQ

Trailing 12 months

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

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