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Kinamed, Inc.

Last updated September 17, 2026

Information

Country: US
Address: 820 Flynn Rd, CAMARILLO, CA, 93012
Website: —
LinkedIn: —
Facebook: —
Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 2027148
DUNS Number: 184896645

Catalogue (346)

Page 4 of 7

Device	Model / Reference	Registries	Class	Status
SuperCable® Grip and Plate System	35-230-4516	FDA UDI	Class II	Active
KineMatch® PFR System	Custom 100	FDA UDI	Class II	Active
NeuroPro® Low Profile	16-1P3-8915	FDA UDI	Class II	Active
NeuroPro®	14-1P3-0700	FDA UDI	Class II	Active
NeuroPro® Low Profile	16-1S1-1604	FDA UDI	Class II	Active
NeuroPro® Low Profile	16-1S1-2004	FDA UDI	Class II	Active
SuperCable® Grip and Plate System	35-230-4532	FDA UDI	Class II	Active
NeuroPro®	14-1T1-0415	FDA UDI	Class I	Unknown
KineMatch® PFR System	22-800-2008	FDA UDI	Class I	Active
SuperCable® ISO-Elastic™ Cerclage System	35-800-3100	FDA UDI	Class I	Active
NeuroPro® Low Profile	16-1P3-4066	FDA UDI	Class II	Active
NeuroPro®	14-1T1-0200	FDA UDI	Class I	Active
SuperCable® ISO-Elastic™ Cerclage System	35-800-3200	FDA UDI	Class I	Active
SuperCable® Grip and Plate System	35-230-4526	FDA UDI	Class II	Active
SuperCable® Iso-Elastic™ Cerclage System	37-100-1010	FDA UDI	Class II	Active
NeuroPro®	14-1S1-2005	FDA UDI	Class II	Active
SuperCable® ISO-Elastic™ Cerclage System	35-800-3030	FDA UDI	Class I	Active
SuperCable® Grip and Plate System	35-234-5014	FDA UDI	Class II	Active
NeuroPro® Low Profile	16-1P3-9013	FDA UDI	Class II	Active
SuperCable® Grip and Plate System	35-234-5020	FDA UDI	Class II	Active
KineMatch® PFR System	22-800-3025	FDA UDI	Class I	Active
KineMatch® PFR System	22-800-4002	FDA UDI	Class I	Active
CarboJet® CO2 Bone Lavage System	25-200-0120	FDA UDI	Class I	Active
SuperCable® ISO-Elastic™ Cerclage System	38-800-3500	FDA UDI	Class I	Active
SuperCable® Grip and Plate System	35-840-1030	FDA UDI	Class I	Active
CarboJet® CO2 Bone Lavage System	25-200-0272	FDA UDI	Class II	Active
NeuroPro®	14-1T1-0410	FDA UDI	Class I	Active
NeuroPro®	14-1P2-0114	FDA UDI	Class II	Active
KineMatch® PFR System	22-800-1022	FDA UDI	Class I	Unknown
NeuroPro® Low Profile	16-1T1-0400	FDA UDI	Class I	Active
SuperCable® Iso-Elastic™ Cerclage System	35-100-1010	FDA UDI	Class II	Active
SuperCable® Grip and Plate System	35-200-1010	FDA UDI	Class II	Active
Multi-Directional Tibial Tubercle Transfer System	23-800-1020	FDA UDI	Class I	Active
NeuroPro® Low Profile	16-1P2-0114	FDA UDI	Class II	Active
SuperCable® ISO-Elastic™ Cerclage System	35-800-3050	FDA UDI	Class I	Active
SuperCable® Grip and Plate System	35-230-4520	FDA UDI	Class II	Active
Multi-Directional Tibial Tubercle Transfer System	23-800-1007	FDA UDI	Class I	Unknown
NeuroPro® Low Profile	16-1P2-0118	FDA UDI	Class II	Active
SuperCable® Grip and Plate System	35-230-4536	FDA UDI	Class II	Active
MD3T™ Multi-Directional Tibial Tubercle Transfer System	23-800-4526	FDA UDI	Class I	Active
KineMatch® PFR System	22-800-2003	FDA UDI	Class I	Active
CarboJet® CO2 Bone Lavage System	25-500-0242	FDA UDI	Class II	Active
KineMatch® PFR System	22-800-2009	FDA UDI	Class I	Active
SuperCable® Grip and Plate System	35-234-5018	FDA UDI	Class II	Active
SuperCable® Grip and Plate System	35-230-4518	FDA UDI	Class II	Active
NeuroPro®	14-1P2-0118	FDA UDI	Class II	Active
SuperCable® Grip and Plate System	35-200-1040	FDA UDI	Class II	Active
KineMatch® PFR System	20-420-0102	FDA UDI	Class II	Active
KineMatch® PFR System	Custom 265	FDA UDI	Class I	Active
NeuroPro®	14-1S1-1635	FDA UDI	Class II	Active

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FDA Recalls (1)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Date	Recall No.	Class	Status	Reason
Aug 18, 2010	Z-2588-2011	—	terminated	The recall was initiated due to inadequate mechanical strength of these screwdrivers' hexagonal tip feature, causing it to strip during final tightening.