Data / Medical devices / United States / Max Neuro Supply Inc.
Max Neuro Supply Inc.: FDA-registered device maker in Diamond Bar, CA, United States, 1 510(k) clearance
Max Neuro Supply Inc. is registered with the FDA (registration 3008588921) in Diamond Bar, CA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated May 16, 2008. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3008588921
- Address
- 1469 Rolling Knoll Rd, Diamond Bar, CA, United States, 91765
- Owner or operator
- Max Neuro Supply Inc. (10033584)
- Roles
- Repackager or relabeler
- First device listed
- September 2, 2010
- Registered through
- 2026
- Brand names listed
- Friendship Medical
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Electrode, Needle | GXZ | 2 | Repackager or relabeler | 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 |
|---|---|---|---|---|---|---|
| May 16, 2008 | K072276 | SUBDERMAL NEEDLE ELECTRODES | GXZ | Substantially Equivalent | Xian Friendship Electronics Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated May 16, 2008. 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.