Data / Medical devices / Canada / Leading Edge MFG. Inc.
Leading Edge MFG. Inc.: FDA-registered device maker in Langley British Columbia, Canada, 1 510(k) clearance
Leading Edge MFG. Inc. is registered with the FDA (registration 3013445676) in Langley British Columbia, Canada. It lists 4 device types. The FDA files 1 510(k) clearance under its listings, the newest dated August 18, 2009. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3013445676
- Address
- E104 - 19720 94A Avenue, Langley British Columbia, Canada, V1M3B7
- Owner or operator
- Leading Edge Mfg. Inc. (10095700)
- Roles
- Manufacturer
- First device listed
- April 15, 2026
- Registered through
- 2026
- Brand names listed
- Cable, electrode, Electroanalgesic delivery system
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Cable, Electrode | IKD | 2 | Manufacturer | accessdata.fda.gov |
| Interferential Current Therapy | LIH | 2 | Manufacturer | accessdata.fda.gov |
| Stimulator, Muscle, Powered | IPF | 2 | Manufacturer | accessdata.fda.gov |
| Stimulator, Nerve, Transcutaneous, For Pain Relief | GZJ | 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 |
|---|---|---|---|---|---|---|
| August 18, 2009 | K083250 | NEUROMED ELECTROANALGESIC DELIVERY SYSTEMS | GZJ | Substantially Equivalent | Aa Neuromed Corp. | accessdata.fda.gov |
Compare with other makers
- All makers of Cable, Electrode
- All makers of Stimulator, Muscle, Powered
- All makers of Stimulator, Nerve, Transcutaneous, For Pain Relief
- All makers of Interferential Current Therapy
Updated August 18, 2009. 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.