Data / Medical devices / China / Maanshan Bond Medical Instruments Co., Ltd.
Maanshan Bond Medical Instruments Co., Ltd.: FDA-registered device maker in Maanshan Anhui, China, 5 510(k) clearances
Maanshan Bond Medical Instruments Co., Ltd. is registered with the FDA (registration 3007699087) in Maanshan Anhui, China. It lists 1 device type. The FDA files 5 510(k) clearances under its listings, the newest dated July 15, 2015. Registered through 2027. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3007699087
- Address
- 1358 Meishan road, Maanshan Economic & Technology Development Zone, Maanshan Anhui, China, 243041
- Owner or operator
- Maanshan Bond Medical Instruments Co., Ltd. (10029216)
- Roles
- Manufacturer
- First device listed
- August 3, 2015
- Registered through
- 2027
- Brand names listed
- Acupotomy Acupuncture Needle, EACU, EACU Acupuncture Needle, JOCU, Pizhen Acupuncture Needle, Renzhen Acupuncture Needle, TeWa 10KB-Type, TeWa 5JB-Type and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Needle, Acupuncture, Single Use | MQX | 2 | 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 |
|---|---|---|---|---|---|---|
| July 15, 2015 | K150903 | EACU, ZAGU, JOCU, EAKU, BALANCE, TEMPO, ACUZONE, SMART, PRIME, ACUSTAR, ACUKING, Myotech Dry, Red Coral Premium, Red Coral J-Type, Red Coral Natural | MQX | Substantially Equivalent | Maanshan Bond Medical Instruments Co., Ltd. | accessdata.fda.gov |
| December 2, 2013 | K132896 | CJ-TYPE: METAL HANDLE WITH GUIDE TUBE, PJ-TYPE: PLASTIC HANDLE WITH GUIDE TUBE, CB-TYPE: METAL HANDLE WITHOUT GUIDE TUBE | MQX | Substantially Equivalent | Asia-Med GmbH and CO KG | accessdata.fda.gov |
| October 14, 2004 | K042063 | PRESS TACK NEEDLE | MQX | Substantially Equivalent | Asia-Med GmbH & Co. Kg. - Werk Suhl | accessdata.fda.gov |
| July 10, 2003 | K031716 | SPECIAL+, S-NEEDLE J-TYPE, S-NEEDLE B-TYPE | MQX | Substantially Equivalent | Asia-Med GmbH and CO KG | accessdata.fda.gov |
| July 10, 2001 | K011808 | ASIA-MED ACUPUNCTURE NEEDLES, (STANDARD, SPECIAL, COMPACT, APEX) | MQX | Substantially Equivalent | Asia-Med GmbH and CO KG | accessdata.fda.gov |
Compare with other makers
Updated July 15, 2015. 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.