Medsource Factory,inc.

Registered establishment in Changzhou, Jiangsu, China. 19 device types.

Registry build 21.09.26

Medsource Factory,inc. is a repacker / relabeller holding a current FDA establishment registration. The registration covers Sheet, Burn, Aid, Transfer and 17 other device types. Its earliest product listing with the FDA dates from 2022.

Registration

FDA registration record for Medsource Factory,inc.
Registered name MEDSOURCE FACTORY,INC.
Status Registered
Registration expires 2026
Registration number 3009512503
FEI number 3009512503
Establishment type Repacker / relabeller, Private-label distributor, Manufacturer, Exporter

Location

Address of Medsource Factory,inc.
City Changzhou
Province Jiangsu
Address NO.160 JIN SHENG DONG LU
Postal code 213200
Country China

What It Makes

Device types Medsource Factory,inc. is registered to make
Device type Class Listed under the names Listed since Chinese makers
Aid, Transfer Class 1 2022 118
Bedding, Disposable, Medical Class 1 2022 308
Blood Pressure Cuff Class 2 2023 50
Connector, Airway (Extension) Class 1 2025 20
Device, Transfer, Patient, Manual Class 1 2022 76
Kit, Surgical Instrument, Disposable Class 1 IV start kit 2024 67
Laryngoscope, Rigid Class 1 2025 44
Light, Examination, Medical, Battery Powered Class 1 2022 53
Orthosis, Truncal/Orthosis, Limb Class 1 2022 68
Pack, Hot Or Cold, Disposable Class 1 2024 176
Regulator, Pressure, Gas Cylinder Class 1 2025 27
Scissors, Medical, Disposable Class 1 2022 36
Sheet, Burn Class 1 Burn Sheet 2025 20
Splint, Extremity, Non-Inflatable, External, Non-Sterile Class 1 2022 62
Strap, Head, Gas Mask Class 1 2022 29
Support, Patient Position Class 1 2024 66
Tape And Bandage, Adhesive Class 1 2025 353
Tourniquet, Nonpneumatic Class 1 2022 124
Valve, Non-Rebreathing Class 2 2022 19

Clearances

No clearance names Medsource Factory,inc. as applicant. 3 are held by other companies and named on this establishment’s own product listings: the device is cleared under that company’s 510(k) and listed under this registration.

510(k) clearances naming Medsource Factory,inc. or its listings
Clearance Decision date Product code Route Held by
K090014 2009-04-09 DXQ Traditional Caremate Medical Device Co., Ltd.
K081516 2008-08-26 CBP Traditional Medsource International, LLC
K052743 2005-12-22 CBP Traditional Dynarex Corp.

Nearby Manufacturers

Other registered manufacturers in the same city
Manufacturer Device types
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Exact Medical Manufacturing, Inc. 17
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Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

The manufacturer named here can complete this record.

Where China Actually Supplies

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2,581device types they are registered for
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