Data / Medical devices / Canada / Eastern Currents Ltd
Eastern Currents Ltd: FDA-registered device maker in Vancouver British Columbia, Canada, 7 510(k) clearances
Eastern Currents Ltd is registered with the FDA (registration 3008264222) in Vancouver British Columbia, Canada. It lists 2 device types. The FDA files 7 510(k) clearances under its listings, the newest dated December 2, 2013. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3008264222
- Address
- 9109 Shaughnessy St., Vancouver British Columbia, Canada, V6P6R9
- Owner or operator
- Eastern Currents Ltd. (10026090)
- Roles
- Complaint file establishment, Exporter to the US, Foreign private label distributor, Manufacturer, Specification developer
- First device listed
- June 6, 2008
- Registered through
- 2026
- Brand names listed
- ASIA MED PRESS TACK NEEDLE, ASIA MED SPECIAL+, ASIA MED S-NEEDLE J-TYPE, ASIA MED S-NEEDLE B-TYPE, ASIA-MED APEX, ASIA-MED COMPACT, ASP SEMI PERMANENT NEEDLES, Acufast -The Earth Friendly Acupuncture Needle, CARBO/OPTIMED BRAND ACUPUNCTURE NEEDLES, Fascia Buddy, Fascia Buddy Square and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Massager, Therapeutic, Manual | LYG | 1 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
| Needle, Acupuncture, Single Use | MQX | 2 | Exporter to the US, Foreign private label distributor, Specification developer | 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 |
|---|---|---|---|---|---|---|
| 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 |
| April 26, 2006 | K060392 | ASP TITANIUM | MQX | Substantially Equivalent | Sedatelec | accessdata.fda.gov |
| December 22, 2005 | K052846 | TEWA CJ-TYPE, PJ-TYPE, CB-TYPE AND PB-TYPE ACUPUNCTURE NEEDLES FOR SINGLE USE | MQX | Substantially Equivalent | Maanshan Medical Instruments Co., Ltd. | 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 |
| February 21, 2003 | K030190 | CARBO/OPTIMED BRAND ACUPUNCTURE NEEDLES | MQX | Substantially Equivalent | Suzhou Sen Sen Medical Supplies , Ltd. | 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 December 2, 2013. 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.