Suzhou Ahno Medical Devices Co., Ltd.

FDA Device Registration & Listing · Suzhou Jiangsu, CN · Registration 3014315669

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
3014315669
FEI Number
3014315669
Entity Name
Suzhou Ahno Medical Devices Co., Ltd.
City/State/Country
Suzhou Jiangsu, CN
Establishment Address
Room B204 No. 8, Baoda Road, Suzhou SIP, Suzhou Jiangsu 215122, CN
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Suzhou Ahno Medical Devices Co., Ltd. (Owner Number: 10056864)
Owner / Operator Contact Address
Room B204 No. 8, Baoda Road, Suzhou SIP, Suzhou, CN-JS 215122, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component Orthopedic Class 2 888.3030 2021-03-25
HRS Plate, Fixation, Bone Orthopedic Class 2 888.3030 2020-03-28
MAX Intervertebral Fusion Device With Bone Graft, Lumbar Orthopedic Class 2 888.3080 2020-01-16
HWE Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment General, Plastic Surgery Class 1 878.4820 2020-03-28
KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component Orthopedic Class 2 888.3030 2020-03-27
HRS Plate, Fixation, Bone Orthopedic Class 2 888.3030 2023-11-12
JDG Prosthesis, Hip, Femoral Component, Cemented, Metal Orthopedic Class 2 888.3360 2019-09-26
HRY Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer Orthopedic Class 2 888.3530 2018-01-24
JDW Pin, Fixation, Threaded Orthopedic Class 2 888.3040 2020-03-28
HWC Screw, Fixation, Bone Orthopedic Class 2 888.3040 2024-01-15
LXH Orthopedic Manual Surgical Instrument Orthopedic Class 1 888.4540 2019-03-19
HWC Screw, Fixation, Bone Orthopedic Class 2 888.3040 2023-04-14
JDW Pin, Fixation, Threaded Orthopedic Class 2 888.3040 2024-03-12
KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component Orthopedic Class 2 888.3030 2024-03-12
JDW Pin, Fixation, Threaded Orthopedic Class 2 888.3040 2024-03-12
KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component Orthopedic Class 2 888.3030 2024-03-12
FZX Guide, Surgical, Instrument General, Plastic Surgery Class 1 878.4800 2023-04-14
JDW Pin, Fixation, Threaded Orthopedic Class 2 888.3040 2024-03-12
HRS Plate, Fixation, Bone Orthopedic Class 2 888.3030 2019-09-25

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

Suzhou Ahno Medical Devices Co., Ltd.
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
K033476 Howmedica Osteonics Corp. MODIFICATION TO HOFFMANN II MICRO EXTERNAL FIXATION SYSTEM 2004-01-20
K042598 Zimmer, Inc. PERIARTICULAR LOCKING PLATES AND SCREWS, 2357 AND 2359 SERIES 2004-10-29
K190842 Jiangsu Trauhui Medical Instrument Co., Ltd. Comus Locking Plate systems 2020-02-03
K130510 Arthrex, Inc. ARTHREX COMPRESSION PLATES 2013-09-25
K202803 Newclip Technics Activmotion S DTO 2021-12-16

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0034-2022 Flower Orthopedics Corporation 2
Flower E-Kit, Advanced-Bone Fixation Fasterner-Fixation of Ref: EWK 201
Z-0009-2008 N/A 2
EPIK KNEE SYSTEM Angled Insert Impactor LM/RL; Catalog #801-03-051 Rev. A; non-sterile; knee prosthesis instrument. Distributed by Encore Medical, L.P., Austin, TX 78758.
Z-0020-2022 Exactech, Inc. 2
OPTETRAK Comprehensive Knee System including OPTETRAK All-polyethylene UNI Tibial Components, Product Lines, 252-12-XX, 252-13-XX, 252-22-XX, 252-23-XX. NOTE: Information reflects Exactech recall expansion initiated on 02/07/2022.
Z-0014-2014 Synthes USA HQ, Inc. 2
Synthes Midfoot Fusion Bolt 6.5 mm. It is indicated for fracture, fixation, osteotomies, nonunions, and fusions of large bones in the foot and ankle.
Z-0026-2013 Orthohelix Surgical Designs Inc 2
OrthoHelix Part #HCS-056-32 3.2MM Cannulated Hex Driver NON STERILE MAT: 465 SS The drivers are used to drive screws in the Mini MaxTorque Screw System, which is intended to be used to stabilize and aid in the fusion of fractures and osteotomies involving small bones of the hand, wrist, afoot, and ankle.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014315669. Last updated year: 2026. Please use registration number 3014315669 when referencing this establishment in official correspondence.
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