Data / Medical devices / Needle, Acupuncture, Single Use / United States
FDA-registered makers of Needle, Acupuncture, Single Use in the United States: 10 establishments
10 establishments in the United States are registered with the FDA to make Needle, Acupuncture, Single Use (product code MQX). 4 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Needle, Acupuncture, Single Use
- Product code
- MQX
- Country
- United States
Makers of Needle, Acupuncture, Single Use in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Health Body World Supply, Inc. Dba The Wabbo Company | Lake Elsinore, CA, United States | Specification developer | 3 | November 13, 2002 | 0 | 0 | 0 | api.fda.gov |
| KM Supplies | Los Angeles, CA, United States | Specification developer | 2 | May 11, 2017 | 0 | 0 | 0 | api.fda.gov |
| Blue Poppy Enterprises | Portland, OR, United States | Specification developer | 1 | July 15, 2015 | 0 | 0 | 0 | api.fda.gov |
| North Coast Medical, Inc. | Morgan Hill, CA, United States | Manufacturer | 1 | January 22, 1998 | 0 | 0 | 0 | api.fda.gov |
| American 3B Scientific | Tucker, GA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Kitotech Medical Inc | Seattle, WA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Marian Monticello | Monticello, IN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Merck Teknika LLC | Durham, NC, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Scientific Molding Corporation, Ltd. Dba SMC Ltd. | Somerset, WI, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tcmzone, LLC | Chandler, AZ, United States | Repackager or relabeler, Reprocessor, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. 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.