VCN TECHNOLOGIES

FDA Device Registration & Listing · SAINT-PRIEST Auvergne-Rhone-Alpes, FR · Registration 9615765

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
9615765
FEI Number
3003756816
Entity Name
VCN TECHNOLOGIES
City/State/Country
SAINT-PRIEST Auvergne-Rhone-Alpes, FR
Establishment Address
57 CHEMIN DE GENAS, SAINT-PRIEST Auvergne-Rhone-Alpes 69800, FR
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
VCN TECHNOLOGIES (Owner Number: 9037877)
Owner / Operator Contact Address
57 CHEMIN DE GENAS, --, SAINT-PRIEST, FR-NOTA 69800, FR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

QUANTUM PIP proximal progressive rasp/PIP distal progressive rasp/MCP proximal progressive rasp/MCP distal progressive rasp LYNC intramedullary implant K-WIRES NEOFUSE NEOSYS IBS large Novastep instrument NEOFUSE QUANTUM TRIWAY NEOFUSE NEOSYS NEOFIT TRIWAY QUANTUM NEOMIS DUAFIT NEOSYS NEOFIT IBS-C/N IBS-C/N IBS S NEOSYS IBS-C/N NEOFUSE TRIWAY NEOSYS TOUCH® CMC 1 TRIWAY Novastep instrument QUANTUM OS2V staples AKILINK OS2VP staples NEOFIT Kirschner wire

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HTW Bit, Drill Orthopedic Class 1 888.4540 2013-12-17
GAC Rasp, Surgical, General & Plastic Surgery General, Plastic Surgery Class 1 878.4800 2026-03-27
HTY Pin, Fixation, Smooth Orthopedic Class 2 888.3040 2017-05-10
FTY Tape, Measuring, Rulers And Calipers General, Plastic Surgery Class 1 878.4800 2022-12-19
FZX Guide, Surgical, Instrument General, Plastic Surgery Class 1 878.4800 2013-12-12
KDD Kit, Surgical Instrument, Disposable General, Plastic Surgery Class 1 878.4800 2022-12-19
HXJ Staple Driver Orthopedic Class 1 888.4540 2013-12-17
GDZ Handle, Scalpel General, Plastic Surgery Class 1 878.4800 2022-12-19
GFG Bit, Surgical General, Plastic Surgery Class 1 878.4820 2013-12-17
HTJ Gauge, Depth Orthopedic Class 1 888.4300 2013-12-17
SFA Prosthesis, Finger, Semi-Constrained, Metal/Polymer Unknown Class 3 N/A 2025-07-21
HWE Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment General, Plastic Surgery Class 1 878.4820 2017-05-10
HTO Reamer Orthopedic Class 1 888.4540 2013-12-17
JDR Staple, Fixation, Bone Orthopedic Class 2 888.3030 2022-12-19
HCF Instrument, Ligature Passing And Knot Tying General, Plastic Surgery Class 1 878.4800 2022-12-19
JDR Staple, Fixation, Bone Orthopedic Class 2 888.3030 2022-12-19
HYA Forceps, Wire Holding General, Plastic Surgery Class 1 878.4800 2025-12-17
HXI Passer, Wire, Orthopedic Orthopedic Class 1 888.4540 2026-03-27

Official Correspondent

Andeol CRISTIN

US Agent Details

Philippe JOLY Business: EASYGMP Email: philippe.joly@easygmp.com Phone: (857) 3898789

Related Public Records

Same Entity

VCN TECHNOLOGIES
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
K895079 Buckman Co., Inc. ACE BEADED K-WIRES ACE OLIVE WIRES 1989-09-13
K922193 Osteo AG OSTEO KIRSCHNER WIRE 1992-07-23
K850026 Kirkstil Corp., Inc. ORTHOPEDIC IMPLANT NAILS & PINS 1985-05-20
K963367 Rms Div. RMS K-WIRE 1996-10-30
K153770 In2bones Sas OS2(R)-VP Varisation Staple 2016-03-21

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0013-05 Biomet, Inc. 2
Lactosorb pin, 2.0 x 20 mm, sterile; ref. 948205.
Z-0039-2018 Teleflex Medical 1
Pilling Knife Handles: a) REF 352950 b) REF 352953 c) REF 352951 d) REF 352957 e) REF 352952 : Reusable surgical knife handles, which are intended for use with blades which are inserted into a slot in the handle.
Z-0021-2015 Biomet, Inc. 1
Compress Face Reamer Product Usage: Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement, tumor resections, revision of previously failed total joint arthroplasty, and trauma.
Z-0008-2023 Synthes (USA) Products LLC 2
Hammertoe Continuous Compression Implant (CCI) Kit Part Number: 46.239.001

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3003431869 HILBRO INTERNATIONAL (PVT) LIMITED SIALKOT Punjab, PK
3023265483 PHEN'X TECHNOLOGIES Chassieu Auvergne-Rhone-Alpes, FR
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 9615765. Last updated year: 2026. Please use registration number 9615765 when referencing this establishment in official correspondence.
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