FDA.report

FLOSPINE LLC

FDA Registration(s)

RegistrationFEINameStatusInitial importerExpiration yearAddress
30115132673011513267FLOSPINE LLC1N2026-01-013998 FAU Blvd Suite 300 Boca Raton FL US 33431

GUDID Contact Samples

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

Source GUDIDProductPhoneEmail
B1830112000010Canaveral® - Polyaxial Set Screw(561) 705-3080info@flospine.com
B1830112450500Canaveral® - Reduction Polyaxial Screw Assembly, 4.5mm x 50mm(561) 705-3080info@flospine.com
B1830171000120Canaveral® - 2.4mm Drill(561)705-3080info@flospine.com

Registered Device Listings

Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1806912003451893K232484KeyLift™ Expandable Interlaminar Stabilization SystemPEK2023-10-19
1806911397082625K223231Ti-Largo Cervical Interbody SystemODP2023-02-24
1806911573922794K210182PANAMA™ Anterior Cervical Plate (ACP) SystemKWQ2021-04-07
1806911969818539K141850FLOSPINE PEDICLE SCREW SYSTEMNKB2014-10-27
1806911016125872
1806911062119193
1806911075434333
1806911116230526
1806911128576359
1806911147603090
1806911171869426
1806911239450917
1806911267698683
1806911371636931
1806911376170051
1806911586021914
1806911677423529
1806911786263676
1806911803873018
1806911807896787
1806911827839842
1806911920069761
1806911938290150
1806912003163079
1806912014001510
1806912030498793

Product Codes Associated With Registrations

Product codeRegistration listing recordsLatest decision
PEK12023-10-19
ODP12023-02-24
KWQ12021-04-07
NKB12014-10-27

PMN

GUDID

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