MedtechSourcebook

Springboard Manufacturing

Contract manufacturer · Rancho Cordova, CA

FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified

FDA registration
3021140368 (openFDA record; or search FDA's registration database)
FEI number
3021140368
Registered for
FDA registration year 2026
Establishment types
Contract manufacturer
Owner or operator
823404997 (FDA owner/operator no. 10094588)
Registered address
2691 Mercantile Dr, Rancho Cordova, CA 95742
Contract listings
10 device listings, 9 product codes, first listed Dec 9, 2025
Certification
Not verified. We have no certification data for this facility yet.

Devices listed as contract work

Each row is an FDA product code this facility lists under its contract establishment type, with the date of its earliest such listing.

Product codeDevice (FDA name)ClassCategoryRoleFirst listed
BZDVentilator, Non-Continuous (Respirator)Class IIAnesthesiologyContract manufacturingDec 9, 2025
DXCClamp, VascularClass IICardiovascularContract manufacturingDec 9, 2025
GCJLaparoscope, General & Plastic SurgeryClass IIGastroenterology and urologyContract manufacturingDec 9, 2025
LITCatheter, Angioplasty, Peripheral, TransluminalClass IICardiovascularContract manufacturingDec 9, 2025
OCCRespiratory Virus Panel Nucleic Acid Assay SystemClass IIMicrobiologyContract manufacturingDec 9, 2025
OZTBalloon Aortic ValvuloplastyClass IICardiovascularContract manufacturingDec 9, 2025
PNOCatheter, Percutaneous, Cutting/ScoringClass IICardiovascularContract manufacturingDec 9, 2025
QOFMulti-Target Respiratory Specimen Nucleic Acid Test Including Sars-Cov-2 And Other Microbial AgentsClass IIMicrobiologyContract manufacturingDec 9, 2025
QQXRespiratory Specimen Nucleic Acid Sars-Cov-2 TestClass IIMicrobiologyContract manufacturingDec 9, 2025