FDA.report

REPUBLIC SPINE

FDA Registration(s)

RegistrationFEINameStatusInitial importerExpiration yearAddress
30117967233011796723REPUBLIC SPINE1N2026-01-01100 NE Third Avenue STE 120 Fort Lauderdale FL US 33301

GUDID Contact Samples

Sampled from matched GUDID device records for this company; this is not an exhaustive company contact directory.

Source GUDIDProductPhoneEmail
B0751000200450Dark Star Deformity - Republic Spine Straight Rod Ø5.5mm x 45mm9542490817rusty@rspine.com
B0751000200450Dark Star Deformity - Republic Spine Straight Rod Ø5.5mm x 45mm561-334-2421james@rspine.com

Registered Device Listings

Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1858811785534023K223096Dark Star Deformity Pedicle Screw SystemNKB2023-05-26
1858811862936075K212028Dark Star Navigation Instrument SystemOLO2021-09-27
1858811816070166K190889Republic Spine Restore Cervical Interbody Fusion SystemODP2019-06-19
1858811991362677K190398Republic Spine Restore Intervertebral Body Fusion SystemMAX2019-09-12
1858811122106713K181495Republic Spine Dark Star Spinal SystemNKB2018-07-25
1858811590390230K150283Republic Spine Dark Star Spinal SystemMNH2015-04-29

Product Codes Associated With Registrations

Product codeRegistration listing recordsLatest decision
NKB22023-05-26
OLO12021-09-27
MAX12019-09-12
ODP12019-06-19
MNH12015-04-29

PMN

GUDID

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