DEVON MEDICAL PRODUCTS (JIANGSU) LTD

FDA Device Registration & Listing · Nantong Jiangsu, CN · Registration 3009538657

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
3009538657
FEI Number
3009538657
Entity Name
DEVON MEDICAL PRODUCTS (JIANGSU) LTD
City/State/Country
Nantong Jiangsu, CN
Establishment Address
No.8 Tongxing Road,Economic & Technological Development Area,226009 Nantong City, Jiangsu, Nantong Jiangsu 226009, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Devon Medical Products (Jiangsu) Ltd (Owner Number: 10053567)
Owner / Operator Contact Address
East Half of 1-2F, Appt D2, 1, Qingfeng Road, Nantong, CN-JS 226017, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Negative pressure wound therapy canisters negative pressure wound therapy Powered suction pump negative pressure wound therapy foot dressing negative pressure wound therapy Powered suction pump Foam Kit

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OMP Negative Pressure Wound Therapy Powered Suction Pump General, Plastic Surgery Class 2 878.4780 2016-12-17
OMP Negative Pressure Wound Therapy Powered Suction Pump General, Plastic Surgery Class 2 878.4780 2016-12-17
OMP Negative Pressure Wound Therapy Powered Suction Pump General, Plastic Surgery Class 2 878.4780 2017-10-09
OMP Negative Pressure Wound Therapy Powered Suction Pump General, Plastic Surgery Class 2 878.4780 2016-12-17
OMP Negative Pressure Wound Therapy Powered Suction Pump General, Plastic Surgery Class 2 878.4780 2016-12-17

Official Correspondent

Neil Cheng

US Agent Details

Knowles Glenn Email: glenn@compressiontherapysystems.com Phone: (770) 6526928

Related Public Records

Same Entity

Devon Medical Products (Jiangsu) Ltd
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0009-2013 Accuro Medical Product LLC 2
Wound Pro Apex Negative Pressure Wound Therapy Powered Suction Pump; Accuro Medical Products LLC, 2854 Hitchcock Ave, Downers Grove, IL 60515; part number 84635400182, sold inside the Apex Negative Wound Therapy system, part number 84635400181 Promotes wound healing through drainage and removal of infectious material and other fluids from the wound site using continuous and/or intermittent negative pressure. Types of wounds indicated include diabetic/neuropathic ulcers, pressure ulcers, chronic wounds, acute wounds and dehisced wounds.
Z-0039-2015 Smith & Nephew, Inc. 2
RENASYS EZ/ RENASYS EZ Plus 250 mL canister with Solidifier Product Usage: RENASYS EZ and RENASYS EZ Plus Canisters are used for the collection of exudate removed from wounds being treated by negative pressure wound therapy (NPWT).
Z-0040-2015 Smith & Nephew, Inc. 2
RENASYS EZ/ RENASYS EZ Plus 800 mL canister with Solidifier Product Usage: RENASYS EZ and RENASYS EZ Plus Canisters are used for the collection of exudate removed from wounds being treated by negative pressure wound therapy (NPWT).
Z-0041-2015 Smith & Nephew, Inc. 2
RENASYS EZ/ RENASYS EZ Plus 800 mL canister (w/o CLP) with Solidifier Product Usage: RENASYS EZ and RENASYS EZ Plus Canisters are used for the collection of exudate removed from wounds being treated by negative pressure wound therapy (NPWT).

Similar Registrations

Registration Number Establishment Name Location
3015143781 VIRTUAL TRUTRENDS TEK.BIL.ILT.SIS.SAN.DAN.EGT.VE TIC.LTD.STI. ankara, TR
3009897021 KCI USA, INC. San Antonio, TX, US
2029275 Sterigenics U.S., LLC Corona, CA, US
3002807523 MEDELA AG BAAR Zug, CH
3030145672 CADENT TECHNOLOGIES, INC. Temecula, CA, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009538657. Last updated year: 2026. Please use registration number 3009538657 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.