510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K152463Substantially Equivalent

SU-POR Patient-Specific Cranial Implant, SU-POR Patient-Specific Facial Implant

Poriferous, LLC, Newnan GA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K152463 is the FDA 510(k) clearance record for SU-POR Patient-Specific Cranial Implant, SU-POR Patient-Specific Facial Implant, a class II device, cleared for Poriferous, LLC on under FDA product code FWP (Prosthesis, Chin, Internal). FDA records list 2 510(k) clearances for Poriferous, LLC, from to . As of , FDA records show no recalls naming K152463.

Clearance record

Decision date
Received
(145 days to decision)
Product code
FWP Prosthesis, Chin, Internal
Regulation
21 CFR 878.3550
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Poriferous, LLC 535 Pine Rd., Suite 206, Newnan GA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code FWP

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