GEORGE TIEMANN & CO.

FDA Device Registration & Listing · HAUPPAUGE, NY, US · Registration 2424531

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
2424531
FEI Number
2424531
Entity Name
GEORGE TIEMANN & CO.
City/State/Country
HAUPPAUGE, NY, US
Establishment Address
25 PLANT AVE., HAUPPAUGE, NY 11788, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
GEORGE TIEMANN & CO. (Owner Number: 2424531)
Owner / Operator Contact Address
25 PLANT AVE., --, Hauppauge, NY 11788, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Retractor, General Tiemann Osteotome, Bone Rongeur, Bone Ronguer, Hand ROSENBLATT Comedone Expressor, extractor Scissor, Dental Skin COBB HURD Surgical clamp general and plastic surgery Forceps, General Bone reduction Clamp Clamp, Inge, HIBBS Scissor, General Surgical HIBBS Surgical tray

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EIG Retractor, All Types Dental Class 1 872.4565 1992-06-26
GFI Osteotome, Manual General, Plastic Surgery Class 1 878.4800 1992-06-26
HTX Rongeur Orthopedic Class 1 888.4540 2012-12-22
EMH Forceps, Rongeur, Surgical Dental Class 1 872.4565 2012-11-26
HRR Scissors, Orthopedic, Surgical Orthopedic Class 1 888.4540 1992-06-26
HNS Expressor Ophthalmic Class 1 886.4350 1992-06-26
EGN Scissors, Surgical Tissue, Dental Dental Class 1 872.4565 2012-11-12
GEG Elevator, Surgical, General & Plastic Surgery General, Plastic Surgery Class 1 878.4800 1992-06-26
GDJ Clamp, Surgical, General & Plastic Surgery General, Plastic Surgery Class 1 878.4800 2012-11-12
HTD Forceps General, Plastic Surgery Class 1 878.4800 1992-06-26
LXH Orthopedic Manual Surgical Instrument Orthopedic Class 1 888.4540 2013-03-22
HXD Clamp General, Plastic Surgery Class 1 878.4800 2012-11-26
EML Chisel, Bone, Surgical Dental Class 1 872.4565 1992-06-26
LRW Scissors, General, Surgical General, Plastic Surgery Class 1 878.4800 2012-11-06
HWA Impactor Orthopedic Class 1 888.4540 1992-06-26
FSM Tray, Surgical, Instrument General, Plastic Surgery Class 1 878.4800 2012-11-12

Official Correspondent

RICHARD MORIARTY

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

GEORGE TIEMANN & CO.
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
K821275 Conphar, Inc. MAYO SCISSOR STRAIGHT 5 1/2 1982-05-28
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 2424531. Last updated year: 2026. Please use registration number 2424531 when referencing this establishment in official correspondence.
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