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RSB SPINE LLC.

US

Last updated September 17, 2026

Information

Country
US
Address
1877 Eagle Pass, Wooster, OH, 44691
Website
—
LinkedIn
—
Facebook
—
Email
—
Phone
—
PRRC Contact
—
EUDAMED SRN
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FDA FEI Number
3003597504
DUNS Number
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Catalogue (126)

Page 3 of 3
DeviceModel / ReferenceRegistriesClassStatus
InterPlate® L-Ti
FDA UDI
Class IActive
InterPlate® L-Ti
FDA UDI
Class IActive
InterPlate® L-Ti
FDA UDI
Class IActive
InterPlate® L-PS
FDA UDI
Class IIActive
InterPlate® C-Ti
FDA UDI
Class IIActive
InterPlate® L-Ti
FDA UDI
Class IIActive
InterPlate® L-PS
FDA UDI
Class IIActive
InterPlate® C-Ti
FDA UDI
Class IActive
InterPlate® C-Ti
FDA UDI
Class IActive
InterPlate® C-PS
FDA UDI
Class IIActive
InterPlate® L-Ti
FDA UDI
Class IIActive
InterPlate® L-Ti
FDA UDI
Class IIActive
InterPlate® L-PS
FDA UDI
Class IIActive
InterPlate® L-Ti
FDA UDI
Class IIActive
InterPlate® C-PS
FDA UDI
Class IIActive
InterPlate® C-PS
FDA UDI
Class IActive
InterPlate® L-Ti
FDA UDI
Class IActive
InterPlate® C-PS
FDA UDI
Class IIActive
InterPlate® L-PS
FDA UDI
Class IActive
Interplate Vbr System K070316
FDA 510(k)
Class IIActive
Interplate Peek Cervical Interbody Fusion Device (ifd) K081194
FDA 510(k)
Class IIActive
Interplate Vbr System K061401
FDA 510(k)
Class IIActive
Modification To: Interplate Vbr System K071372
FDA 510(k)
Class IIActive
C-Ps Peek Optima Cervical Interbody Spacer, L-Ps Peek Optima Lumbar Interbody Spacer K092540
FDA 510(k)
Class IIActive
Interplate Interbody Fusion Device, Models C, Cgc, L And Lgc K071922
FDA 510(k)
Class IIActive
Interplate C K092070
FDA 510(k)
Class IIActive

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