Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3030680364

FEI Number

3030680364

Entity Name

SHANGHAI NUOFENG MEDICAL TECHNOLOGY CO., LTD.

City/State/Country

Shanghai, CN

Establishment Address

Building 5 No 128 Jina An Road, Feng Hing Town, Jin Shan Dist, Shanghai 201502, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Shanghai NuoFeng Medical Technology Co., Ltd. (Owner Number: 10090207)

Owner / Operator Contact Address

Building 5 No 128 Jina An Road, Feng Hing Town, Jin Shan Dist, Shanghai, CN-SH 201502, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Face Protector Body Positioners Boot Liner Head Rest Foam Pads Foam Positioners Straps Covers Arm Protectors Wedges ProneSafe Foam Head Rest Nasotracheal Tube Immobilizer (NTI) Tube Holder Air Assist Power Lift Pink Pad Air Assist Mattress Microfiber Cloth Tray Corner Protector Polybag Trocar Swab Suture Bag Mop Heads Absorbent Mats Antifatigue Mats Foot Pedal Bags Kit Accessories OR Turnover Kit EZ Kits

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
CCX	Support, Patient Position	Anesthesiology	Class 1	868.6820	2024-02-28
KGX	Tape And Bandage, Adhesive	General Hospital	Class 1	880.5240	2024-03-01
FMR	Device, Transfer, Patient, Manual	General Hospital	Class 1	880.6785	2024-03-01
MDM	Instrument, Manual, Surgical, General Use	General, Plastic Surgery	Class 1	878.4800	2024-03-01
FRL	Fiber, Medical, Absorbent	General Hospital	Class 1	880.5300	2024-03-01
KDD	Kit, Surgical Instrument, Disposable	General, Plastic Surgery	Class 1	878.4800	2024-03-01

Official Correspondent

Ye Chen

US Agent Details

Paul Lloyd Business: XODUS MEDICAL INC Email: plloyd@xodusmedical.com Phone: (724) 3375500

Related Public Records

Same Entity

Shanghai NuoFeng Medical Technology 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
K843874	Beiersdorf, Inc.	LEUKOPOR SURGICAL TAPE	1985-02-21
K915446	Sun Glitz Corp.	STRETCH WRAP	1992-05-06
K833120	Acme United Corp.	ONE TIME COMPOUND BENZOIN TINCTURE-	1983-12-29
K870091	Avery Intl.	IV SECUREMENT DEVICE USING PCCE THERMO. FILM	1987-02-04

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3007441485	MOSER-BAER AG	Sumiswald Bern, CH
3003495693	EMERALD NONWOVENS INTL. CO., LTD.	Phetchaburi, TH
3012226300	AVILIGN MEDICAL	Sialkot Punjab, PK

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3030680364. Last updated year: 2026. Please use registration number 3030680364 when referencing this establishment in official correspondence.