Data / Medical devices / Canada / Wasip Ltd.
Wasip Ltd.: FDA-registered device maker in TORONTO Ontario, Canada, 1 510(k) clearance
Wasip Ltd. is registered with the FDA (registration 3004018264) in TORONTO Ontario, Canada. It lists 10 device types. The FDA files 1 510(k) clearance under its listings, the newest dated January 22, 1988. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3004018264
- Address
- 3771 Victoria Park Ave., TORONTO Ontario, Canada, M1W 3Z5
- Owner or operator
- WASIP LTD. (9059421)
- Roles
- Complaint file establishment, Foreign private label distributor, Manufacturer, Repackager or relabeler
- First device listed
- January 4, 2008
- Registered through
- 2026
- Brand names listed
- 10 x 10cm Burn Dressing, 0404-60, 15000012 P24 Florida School Bus Kit, F93P24053, 15000013 P24 Indiana School Bus Kit , F93P24052, 20 x 20cm Burn Dressing, 0808-30, 30 x 30cm Burn Dressing, 1212-20, 5 x 15cm Burn Dressing, 0206-60, 55 Piece First Aid Kit, FAK55-N, ANSI-2015 Class A 10 Person Kit, Plastic, ANSI15-10 and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Bedding, Disposable, Medical | KME | 1 | Complaint file establishment, Foreign private label distributor, Manufacturer | accessdata.fda.gov |
| Dressing, Wound, Drug | FRO | U | Complaint file establishment, Foreign private label distributor, Repackager or relabeler | accessdata.fda.gov |
| Dressing, Wound, Hydrogel Without Drug And/Or Biologic | NAE | 1 | Foreign private label distributor | accessdata.fda.gov |
| First Aid Kit With Drug | LRR | N | Complaint file establishment, Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| First Aid Kit Without Drug | OHO | 1 | Complaint file establishment, Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Mask, Oxygen | BYG | 1 | Complaint file establishment, Foreign private label distributor, Manufacturer | accessdata.fda.gov |
| Mask, Oxygen, Non-Rebreathing | KGB | 1 | Complaint file establishment, Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Splint, Hand, And Components | ILH | 1 | Complaint file establishment, Foreign private label distributor, Manufacturer | accessdata.fda.gov |
| Stretcher, Hand-Carried | FPP | 1 | Foreign private label distributor | accessdata.fda.gov |
| Tape And Bandage, Adhesive | KGX | 1 | Complaint file establishment, Foreign private label distributor, Manufacturer, 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 |
|---|---|---|---|---|---|---|
| January 22, 1988 | K864841 | WATER-JEL(R) BURN DRESSING | FRO | Substantially Equivalent for Some Indications | Trilling Resources, Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Bedding, Disposable, Medical
- All makers of Splint, Hand, And Components
- All makers of First Aid Kit Without Drug
- All makers of Mask, Oxygen, Non-Rebreathing
- All makers of Dressing, Wound, Hydrogel Without Drug And/Or Biologic
- All makers of Stretcher, Hand-Carried
Updated January 22, 1988. 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.