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Sign in to claim this brandGLOBAL PROTECTION CORP.
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 630 Lynnway, Lynn, MA, 01905
- Website
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- —
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- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 1222115
- DUNS Number
- —
Catalogue (814)
Page 17 of 17| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Custom Condoms | CC-BC01 | FDA UDI | Class II | Active |
| ONE Super Sensitive | 11609 | FDA UDI | Class II | Active |
| My One | MYONE-51E | FDA UDI | Class II | Active |
| ONE Nitrile Condom | K240896 | FDA 510(k) | Class II | Active |
| Male Latex Condom | K203536 | FDA 510(k) | Class II | Active |
| Knight Light Nonlubricated Condom | K960552 | FDA 510(k) | Class II | Active |
| Water-based Lubricant | K250142 | FDA 510(k) | Class II | Active |
| Non-spermicidal Lubricated Male Latex Condom | K193578 | FDA 510(k) | Class II | Active |
| ONE Nitrile Condom | K243967 | FDA 510(k) | Class II | Active |
| ONE Male Condom | DEN210034 | FDA 510(k) | Class II | Active |
| Powder-Free Nitrile Examination Gloves | K223214 | FDA 510(k) | Class I | Active |
| Plain Water-based Lubricant | K243972 | FDA 510(k) | Class II | Active |
| Latex Condom And Latex Condom Lubricated With Nonoxynol-9 | K024324 | FDA 510(k) | Class II | Active |
| Natural Rubber Latex Ultrasound Transducer Probe Covers | K213087 | FDA 510(k) | Class II | Active |
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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 |
|---|---|---|---|---|
| Sep 11, 2007 | Z-0054-2008 | — | terminated | Condoms fail the water leak test and package integrity |