ULRICH AG

FDA Device Registration & Listing · ST. GALLEN Sankt Gallen, CH · Registration 8039053

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
8039053
FEI Number
5639
Entity Name
ULRICH AG
City/State/Country
ST. GALLEN Sankt Gallen, CH
Establishment Address
MOEVENSTRASSE 12, ST. GALLEN Sankt Gallen 9015, CH
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
ULRICH AG (Owner Number: 8039053)
Owner / Operator Contact Address
MOEVENSTRASSE 12, --, ST. GALLEN, CH-NOTA 9015, CH
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Ulrich Swiss Ulrich Swiss Ulrich Swiss Ulrich Swiss Ulrich Swiss Ulrich Swiss Ulrich Swiss Ulrich Swiss Ulrich Swiss Ulrich Swiss Ulrich Swiss Ulrich Swiss Ulrich Swiss Ulrich Swiss

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HTE Elevator General, Plastic Surgery Class 1 878.4800 1996-07-05
GDH Gouge, Surgical, General & Plastic Surgery General, Plastic Surgery Class 1 878.4800 1996-07-05
LXH Orthopedic Manual Surgical Instrument Orthopedic Class 1 888.4540 1996-07-05
ILH Splint, Hand, And Components Physical Medicine Class 1 890.3475 2010-03-30
HTF Curette General, Plastic Surgery Class 1 878.4800 1996-07-05
GAD Retractor General, Plastic Surgery Class 1 878.4800 1996-07-05
HXX Screwdriver Orthopedic Class 1 888.4540 1996-07-05
HTX Rongeur Orthopedic Class 1 888.4540 1996-07-05
HWM Osteotome General, Plastic Surgery Class 1 878.4800 1996-07-05
HXS Twister, Wire Orthopedic Class 1 888.4540 1996-07-05
DWS Instruments, Surgical, Cardiovascular Cardiovascular Class 1 870.4500 1983-09-27
FZO Chisel, Surgical, Manual General, Plastic Surgery Class 1 878.4800 1996-07-05
HTD Forceps General, Plastic Surgery Class 1 878.4800 1983-09-27
EML Chisel, Bone, Surgical Dental Class 1 872.4565 1996-07-05

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

ULRICH AG
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
K922626 Andronic Devices, Ltd. ADEPT INSTRUMENT POSITIONING ACCESSORY 1992-10-19
K820290 The Anspach Effort, Inc. SELF RETAINING RETRACTOR FOR HAND SURG 1982-03-05
K760422 Cutter Laboratories, Inc. SURGICAL RETRACTOR 1976-08-23
K852723 The Huxley Instrument Corp. FOERSTER SPONGE FORCEPS, SERRATED, 7+SS 410 OR 420 1985-07-15
K873512 Arthropedics, Inc. SERRATED GRASPING FORCEPS, RIGHT 1987-11-02

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0009-2007 Smith & Nephew Inc 1
Journey Nonporous Fin-Stem Tibial Punch, Catalog Numbers: 74018811, 74018813, 74018815, 74018817.
Z-0010-2007 Smith & Nephew Inc 1
Genesis II Nonporous Fin-Stem Tibial Punch, Catalog Numbers: 71440480, 71440482, 71440484, 71440486
Z-0011-06 Stryker Howmedica Osteonics Corp. 1
Allocraft TLIF Bone Inserter.
Z-0011-2007 Smith & Nephew Inc 1
Genesis II Oversized Nonporous Fin-Stem Tibial Punch, Catalog Numbers: 71927102, 71927103, 71927104, 71927105
Z-0013-2011 Depuy Orthopaedics, Inc. 1
Summit Broach Handle, NON-STERILE, MFG: DEPUY ORTHOPAEDICS, INC., PO BOX 988 WARSAW, IN 46581, 1 800 366 8143 Catalog Number: 2570-00-000 The Summit Broach Handle (instrumentation) is used with the DePuy Summit Tapered Hip System. The Broach Handle is used to prepare the femur for hip system implantation. The broach handle is an impaction/extraction device that holds broaches for creating the cavity in the femur during hip arthroplasty.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 8039053. Last updated year: 2026. Please use registration number 8039053 when referencing this establishment in official correspondence.
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