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GENESISBPS LLC

US

Last updated September 17, 2026

Information

Country
US
Address
400 Corporate Dr, Mahwah, NJ, 07430
Website
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LinkedIn
—
Facebook
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Email
—
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)

DeviceModel / ReferenceRegistriesClassStatus
RapidWeld Blade Module Kit GRW-430
FDA UDI
Class IIActive
TCD B40 Wafers TCD B40
FDA UDI
Class IIActive
Genesis RapidWeld STW Sterile Tube Welder GRW-430
FDA UDI
Class IIActive
Genesis Tube Stripper HS-002
FDA UDI
Class IActive
TCD B40 Wafers TCD B40
FDA UDI
Class IIActive
Genesis RapidWeld II STW Sterile Tube Welder GRW-430-02
FDA UDI
Class IIActive
RapidWeld Blade Module Kit GRW-430
FDA UDI
Class IIActive
RapidWeld Blade Module Kit GRW-430
FDA UDI
Class IIActive
Total Containment Device (TCD) TCD B40
FDA UDI
Class IIActive
Flu-Admin, Models 60150, 60150c, 60151c, 60153c, 60160 K082027
FDA 510(k)
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

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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.

DateRecall No.ClassStatusReason
Jul 17, 2014Z-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, 2014Z-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, 2014Z-2667-2014—terminated

Genesis BPS is recalling numerous devices since they did not notify the agency of its intent to introduce material changes.