PORIFEROUS, LLC

FDA Device Registration & Listing · Newnan, GA, US · Registration 3010781616

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3010781616
FEI Number
3010781616
Entity Name
PORIFEROUS, LLC
City/State/Country
Newnan, GA, US
Establishment Address
535 PINE RD STE 206, Newnan, GA 30263, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Poriferous LLC (Owner Number: 10046093)
Owner / Operator Contact Address
535 Pine Road, Suite 206, Newnan, GA 30263, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

SU-POR Patient-Specific Cranial Implant, SU-POR Patient Specific Facial Implant Su-Por Surgial Implant Su-Por Surgical Cutting Guide

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MDM Instrument, Manual, Surgical, General Use General, Plastic Surgery Class 1 878.4800 2014-01-31
FWP Prosthesis, Chin, Internal General, Plastic Surgery Class 2 878.3550 2016-03-21
FWP Prosthesis, Chin, Internal General, Plastic Surgery Class 2 878.3550 2014-06-18
KKY Material, Polytetrafluoroethylene Vitreous Carbon, For Maxillofacial Reconstruction General, Plastic Surgery Class 2 878.3500 2014-06-18
HWT Template Orthopedic Class 1 888.4800 2020-06-17

Official Correspondent

Aaron Noble

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Poriferous LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K080507 Ceremed , Inc. AOC POROUS POLYETHYLENE, AOC POROUS HDPE, AOC POROUS POLYETHYLENE SURGICAL IMPLANT 2008-04-21

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010781616. Last updated year: 2026. Please use registration number 3010781616 when referencing this establishment in official correspondence.
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