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Sign in to claim this brandPROCEDURE PRODUCTS, INC.
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 1801 WEST 4TH PLAIN BLVD., Vancouver, WA, 98660
- Website
- —
- —
- —
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- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3020778
- DUNS Number
- —
Catalogue (116)
Page 3 of 3| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Insufflator Connecting Filter | K923194 | FDA 510(k) | Class II | Active |
| Bag Spigot | K910673 | FDA 510(k) | Class II | Active |
| Torque Device | K922536 | FDA 510(k) | Class II | Active |
| Material Addition Lexan & K-Resin | K833554 | FDA 510(k) | Class II | Active |
| Connecting Set | K914128 | FDA 510(k) | Class II | Active |
| Cervical Spatula | K811548 | FDA 510(k) | Class II | Active |
| Male Luer Lock Plugs | K810921 | FDA 510(k) | Class II | Active |
| 10cc Syringe Control Ring Set | K874747 | FDA 510(k) | Class II | Active |
| Glass Syringes, Drug, Luer Lock | K820384 | FDA 510(k) | Class II | Active |
| Freedom Syringe | K161812 | FDA 510(k) | Class II | Active |
| Angio Waste Fluids Dump Bag | K874037 | FDA 510(k) | Class II | Active |
| Injection Cap, Luer Lock | K812657 | FDA 510(k) | Class II | Active |
| Modified 10cc Syringe Control Ring Set | K884985 | FDA 510(k) | Class II | Active |
| Disposable Stopcocks | K842173 | FDA 510(k) | Class II | Active |
| Single Use Seldinger/Cournand Perc. Ndl | K810859 | FDA 510(k) | Class II | Active |
| Custom Coronary Manifold Kits | K853749 | FDA 510(k) | Class II | Active |
Related Companies
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FDA Recalls (1)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Oct 27, 2015 | Z-0355-2016 | — | terminated | The firm had received a complaint alleging that a medical professional had difficulty inserting a guide wire into a needle |