RYDER ELECTRONICS (XINFENG) LTD.

FDA Device Registration & Listing · Ganzhou City Jiangxi, CN · Registration 3017643003

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
3017643003
FEI Number
3017643003
Entity Name
RYDER ELECTRONICS (XINFENG) LTD.
City/State/Country
Ganzhou City Jiangxi, CN
Establishment Address
East Shuidong Avenue, Industrial Park, Xinfeng Town, Ganzhou City Jiangxi 341600, CN
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Ryder Electronics (Xinfeng) Ltd. (Owner Number: 10079144)
Owner / Operator Contact Address
East Shuidong Avenue, Industrial Park, Xinfeng Town, Ganzhou City, CN-JX 341600, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Normatec 3 Normatec Go Normatec 2 Pro Normatec 2 Normatec Elite

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IRP Massager, Powered Inflatable Tube Physical Medicine Class 2 890.5650 2022-03-25
IRP Massager, Powered Inflatable Tube Physical Medicine Class 2 890.5650 2022-07-18
IRP Massager, Powered Inflatable Tube Physical Medicine Class 2 890.5650 2020-11-20
IRP Massager, Powered Inflatable Tube Physical Medicine Class 2 890.5650 2024-04-14

Official Correspondent

Niki xu

US Agent Details

Steve Henderson Business: NormaTec Industries, LP. Email: regulatory@hyperice.com Phone: (949) 5654994

Related Public Records

Same Entity

Ryder Electronics (Xinfeng) 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
K242140 Jiale Health Technology Shenzhen Co., Ltd. Air Compression Leg Massager (K-705) 2025-03-17

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017643003. Last updated year: 2026. Please use registration number 3017643003 when referencing this establishment in official correspondence.
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