CHARLES PERY & CIE

FDA Device Registration & Listing · SCIONZIER Haute-Savoie, FR · Registration 9615800

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
9615800
FEI Number
3003051987
Entity Name
CHARLES PERY & CIE
City/State/Country
SCIONZIER Haute-Savoie, FR
Establishment Address
360 avenue du stade, SCIONZIER Haute-Savoie 74950, FR
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Charles PERY & Cie (Owner Number: 10043431)
Owner / Operator Contact Address
360 avenue du stade, SCIONZIER, FR-74 74950, FR
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
LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented Orthopedic Class 2 888.3353 2013-03-18
MEH Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate Orthopedic Class 2 888.3353 2013-03-18
HRS Plate, Fixation, Bone Orthopedic Class 2 888.3030 2013-12-06
LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented Orthopedic Class 2 888.3353 2018-12-19
MEH Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate Orthopedic Class 2 888.3353 2018-12-19
HRS Plate, Fixation, Bone Orthopedic Class 2 888.3030 2013-12-06

Official Correspondent

anicet TEDZEMBONG TEKEMETIEU

US Agent Details

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

Related Public Records

Same Entity

Charles PERY & Cie
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
K030151 Hayes Medical, Inc. CONSENSUS HIP SYSTEM, UNISYN HIP SYSTEM 2003-04-10
K153381 Corin U.S.A. Limited Corin Metafix Hip Stem 2016-01-21
K140975 Lima Corporate S.P.A. MASTERSL FEMORAL STEM 2014-06-10
K932222 Dow Corning Wright SLT FEMORAL HEAD 1994-05-27
K910547 Turnkey Intergration USA, Inc. FELDMUEHLE CERAMIC HEAD (12/14 X 28MM) 1991-04-12

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

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 9615800. Last updated year: 2026. Please use registration number 9615800 when referencing this establishment in official correspondence.
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