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Sign in to claim this brandGENESISBPS LLC
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 400 Corporate Dr, Mahwah, NJ, 07430
- Website
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- Phone
- —
- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
- 1000527169
- DUNS Number
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Catalogue (10)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| RapidWeld Blade Module Kit | GRW-430 | FDA UDI | Class II | Active |
| TCD B40 Wafers | TCD B40 | FDA UDI | Class II | Active |
| Genesis RapidWeld STW Sterile Tube Welder | GRW-430 | FDA UDI | Class II | Active |
| Genesis Tube Stripper | HS-002 | FDA UDI | Class I | Active |
| TCD B40 Wafers | TCD B40 | FDA UDI | Class II | Active |
| Genesis RapidWeld II STW Sterile Tube Welder | GRW-430-02 | FDA UDI | Class II | Active |
| RapidWeld Blade Module Kit | GRW-430 | FDA UDI | Class II | Active |
| RapidWeld Blade Module Kit | GRW-430 | FDA UDI | Class II | Active |
| Total Containment Device (TCD) | TCD B40 | FDA UDI | Class II | Active |
| Flu-Admin, Models 60150, 60150c, 60151c, 60153c, 60160 | K082027 | FDA 510(k) | Class II | Active |
Related Companies
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Authorities
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FDA Recalls (3)
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 |
|---|---|---|---|---|
| Jul 17, 2014 | Z-2668-2014 | — | terminated | Genesis BPS is recalling numerous devices since they did not notify the agency of its intent to introduce material changes. |
| Jul 17, 2014 | Z-2669-2014 | — | terminated | Genesis BPS is recalling numerous devices since they did not notify the agency of its intent to introduce material changes. |
| Jul 17, 2014 | Z-2667-2014 | — | terminated | Genesis BPS is recalling numerous devices since they did not notify the agency of its intent to introduce material changes. |