Data / Medical devices / Canada / Walsh Medical Devices, Inc.
Walsh Medical Devices, Inc.: FDA-registered device maker in OAKVILLE Ontario, Canada, 1 510(k) clearance
Walsh Medical Devices, Inc. is registered with the FDA (registration 9680660) in OAKVILLE Ontario, Canada. It lists 5 device types. The FDA files 1 510(k) clearance under its listings, the newest dated July 17, 2003. Registered through 2027. FDA data exported November 3, 2026.
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- FDA registration number
- 9680660
- FEI number
- 3002808473
- Address
- 1200 South Service RD. West Unit 3, OAKVILLE Ontario, Canada, L6L 5T7
- Owner or operator
- WALSH MEDICAL DEVICES, INC. (9010481)
- Roles
- Manufacturer
- First device listed
- May 25, 1994
- Registered through
- 2027
- Brand names listed
- CRAWFORD LACRIMAL INTUBATION SET (W, Lacrimal Light Probe Fiberoptic, SLING, T SUTURE), TIP, WALSH MEDICAL DEVICES INC. CAUTERY, WITHOUT SUTURE), WRIGHT PTOSIS SUPPORT
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Apparatus, Cautery, Radiofrequency, Ac-Powered | HQR | 2 | Manufacturer | accessdata.fda.gov |
| Crutch, Ptosis | HJZ | 1 | Manufacturer | accessdata.fda.gov |
| Dilator, Lachrymal | HNW | 1 | Manufacturer | accessdata.fda.gov |
| Electrosurgical, Cutting & Coagulation & Accessories | GEI | 2 | Manufacturer | accessdata.fda.gov |
| Transilluminator, Battery-Powered | HJN | 1 | 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 17, 2003 | K030158 | UNIT, CAUTERY, TEHRMAL,BATTERY-POWERED | GEI | Substantially Equivalent | Walsh Medical Devices, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Electrosurgical, Cutting & Coagulation & Accessories
- All makers of Apparatus, Cautery, Radiofrequency, Ac-Powered
- All makers of Transilluminator, Battery-Powered
- All makers of Dilator, Lachrymal
- All makers of Crutch, Ptosis
Updated July 17, 2003. 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.