510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K863565Substantially Equivalent

Mentor Alloplastic Spermatocele

Mentor, Goleta CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K863565 is the FDA 510(k) clearance record for MENTOR ALLOPLASTIC SPERMATOCELE, cleared for Mentor Corp. on under FDA product code LQS (Spermatocele, Alloplastic). FDA records list 65 510(k) clearances for Mentor Corp., from to . As of , FDA records show no recalls naming K863565.

Clearance record

Decision date
Received
(68 days to decision)
Product code
LQS Spermatocele, Alloplastic
Device class
Unclassified
Review panel
Unknown
Applicant
Mentor Corp. 600 Pine Ave., Goleta CA
Third party review
No

Clearances, product code LQS

Trailing 12 months

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

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