Data / Medical devices / China / Suzhou Shenlong Medical Apparatus Co., Ltd.
Suzhou Shenlong Medical Apparatus Co., Ltd.: FDA-registered device maker in Suzhou Jiangsu, China, 1 510(k) clearance
Suzhou Shenlong Medical Apparatus Co., Ltd. is registered with the FDA (registration 3003152436) in Suzhou Jiangsu, China. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated February 14, 2003. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3003152436
- Address
- No. 32 Xupai Road Xuguan Industrial Park, Suzhou Jiangsu, China, 215151
- Owner or operator
- Suzhou Shenlong Medical Apparatus Co., Ltd. (10039267)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- December 21, 2011
- Registered through
- 2026
- Brand names listed
- Bio-North Flex Magnet 1" R, Bio-North Flex Magnet 1.5"R, Bio-North Flex Magnet 2" R, Bio-North Flex Magnet 2x3.5", Bio-North Flex Magnet 3" R, Bio-North Flex Magnet 4x6", Disposable Cup 2.3 cm, 2 pcs/pkt, Disposable Cup 2.8 cm, 2 pcs/pkt and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Device, Pressure Applying | KNM | 1 | Manufacturer | accessdata.fda.gov |
| Needle, Acupuncture, Single Use | MQX | 2 | Manufacturer | accessdata.fda.gov |
| Pack, Heat, Moist | IMA | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| February 14, 2003 | K023787 | TAI-CHI AND MASTER ACUPUNCTURE NEEDLES | MQX | Substantially Equivalent | Lhasa Medical, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Needle, Acupuncture, Single Use
- All makers of Pack, Heat, Moist
- All makers of Device, Pressure Applying
Updated February 14, 2003. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.