PFM MEDICAL MSG GMBH

FDA Device Registration & Listing · Nonnweiler Saarland, DE · Registration 3026560514

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
3026560514
FEI Number
3026560514
Entity Name
PFM MEDICAL MSG GMBH
City/State/Country
Nonnweiler Saarland, DE
Establishment Address
Am Soterberg 4, Nonnweiler Saarland 66620, DE
Establishment Type(s)
Sterilize Medical Device for Another Party (Contract Sterilizer)
Owner / Operator
pfm medical msg gmbh (Owner Number: 10094746)
Owner / Operator Contact Address
1916 Palomar Oaks Way, Suite 150, Carlsbad, CA 92008, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

NitOcclud TPort Jet Port Asept TiMesh

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MAE Occluder, Patent Ductus, Arteriosus Unknown Class 3 N/A 2025-12-19
LJT Port & Catheter, Implanted, Subcutaneous, Intravascular General Hospital Class 2 880.5965 2025-12-19
LJT Port & Catheter, Implanted, Subcutaneous, Intravascular General Hospital Class 2 880.5965 2025-12-19
KDQ Bottle, Collection, Vacuum General Hospital Class 2 880.6740 2025-12-19
OXJ Mesh, Surgical, Non-Absorbable, Large Abdominal Wall Defects General, Plastic Surgery Class 2 878.3300 2025-12-19
FTL Mesh, Surgical, Polymeric General, Plastic Surgery Class 2 878.3300 2025-12-19

Official Correspondent

Jessica Jho

US Agent Details

Jessica Jho Email: jjho@pfmmedicalusa.com Phone: (801) 4559267

Related Public Records

Same Entity

pfm medical msg gmbh
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
K912423 Med Institute, Inc. VITAL-PORT M.R.I. VASCULAR ACCESS SYSTEM 7012,7112 1991-07-30
K961652 Arrow Intl., Inc. LOW PROFILE PLASTIC PORT DETACHED CATHETER SYSTEM CATALOG #1017 1996-07-19
K893460 Therex Corp. A-PORT IMPLANT VASCULAR ACCESS SYSTEM .6MM/2.29MM 1989-06-23
K220540 Covidien ProGrip Self-Gripping Polypropylene Mesh 2022-09-22

Similar Registrations

Registration Number Establishment Name Location
3007113487 Abbott Medical Saint Paul, MN, US
3014918977 Abbott Medical Costa Rica Limitada (Structural Heart) El Coyol Alajuela, CR
1928237 MIDWEST STERILIZATION CORP. JACKSON, MO, US
3012179728 St. Jude Medical Roseville, MN, US
2135147 Abbott Medical Plymouth, MN, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3026560514. Last updated year: 2026. Please use registration number 3026560514 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.