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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 6 of 7

Device	Model / Reference	Registries	Class	Status
SuperCable® Grip and Plate System	35-850-2012	FDA UDI	Class I	Active
SuperCable® Grip and Plate System	35-220-3012	FDA UDI	Class II	Active
NeuroPro®	14-1DM-1605	FDA UDI	Class I	Active
NeuroPro®	14-1P1-0211	FDA UDI	Class II	Active
NeuroPro®	14-1T1-0220	FDA UDI	Class I	Active
SuperCable® Grip and Plate System	35-850-2010	FDA UDI	Class I	Active
SuperCable® Grip and Plate System	35-234-5022	FDA UDI	Class II	Active
NeuroPro®	14-1T1-0310	FDA UDI	Class I	Active
NeuroPro®	14-1T1-0100	FDA UDI	Class I	Active
SuperCable® Grip and Plate System	35-860-1030	FDA UDI	Class I	Active
SuperCable® Grip and Plate System	35-234-5030	FDA UDI	Class II	Active
SuperCable® ISO-Elastic™ Cerclage System	CUSTOM 372	FDA UDI	Class I	Active
NeuroPro®	14-1S4-1605	FDA UDI	Class II	Active
CarboJet® CO2 Bone Lavage System	25-500-0246	FDA UDI	Class II	Active
KineMatch® PFR System	22-800-2005	FDA UDI	Class I	Active
CarboJet XF® Bone Preparation System	27-200-2000	FDA UDI	Class II	Active
NeuroPro®	14-1DJ-1605	FDA UDI	Class I	Active
CarboJet® CO2 Bone Lavage System	25-200-0280	FDA UDI	Class II	Unknown
SuperCable® ISO-Elastic™ Cerclage System	35-800-4000	FDA UDI	Class I	Active
SuperCable® Grip and Plate System	35-230-4545	FDA UDI	Class II	Active
KineMatch® PFR System	22-800-3018	FDA UDI	Class I	Active
SuperCable® Grip and Plate System	35-230-4510	FDA UDI	Class II	Active
NeuroPro® Low Profile	16-1P1-0812	FDA UDI	Class II	Active
CarboJet® CO2 Bone Lavage System	25-200-0281	FDA UDI	Class II	Unknown
NeuroPro® Low Profile	16-1P1-3183	FDA UDI	Class II	Active
NeuroPro®	14-1DG-1605	FDA UDI	Class I	Active
SuperCable® ISO-Elastic™ Cerclage System	35-800-1002	FDA UDI	Class I	Active
SuperCable® ISO-Elastic™ Cerclage System	35-800-3202	FDA UDI	Class I	Active
NeuroPro®	14-1S1-1606	FDA UDI	Class II	Active
NeuroPro® Low Profile	16-1S3-1635	FDA UDI	Class II	Active
NeuroPro®	14-1P3-0650	FDA UDI	Class II	Active
SuperCable® ISO-Elastic™ Cerclage System	35-880-3060	FDA UDI	Class I	Active
SuperCable® Grip and Plate System	35-234-5045	FDA UDI	Class II	Active
KineMatch® PFR System	Custom 261	FDA UDI	Class I	Active
KineMatch® PFR System	20-420-0101	FDA UDI	Class II	Active
SuperCable® ISO-Elastic™ Cerclage System	35-880-2040	FDA UDI	Class I	Active
NeuroPro®	14-1T1-0350	FDA UDI	Class I	Unknown
MD3T™ Multi-Directional Tibial Tubercle Transfer System	23-800-1002	FDA UDI	Class I	Active
NeuroPro® Low Profile	16-1P3-1045	FDA UDI	Class II	Active
CarboJet® CO2 Bone Lavage System	25-200-0274	FDA UDI	Class II	Active
SuperCable® Grip and Plate System	35-200-1020	FDA UDI	Class II	Active
NeuroPro®	14-1P2-0122	FDA UDI	Class II	Active
KineMatch® PFR System	22-800-2012	FDA UDI	Class I	Active
KineMatch® PFR System	22-800-3019	FDA UDI	Class I	Active
MD3T™ Multi-Directional Tibial Tubercle Transfer System	23-800-1028	FDA UDI	Class I	Active
MD3T™ Multi-Directional Tibial Tubercle Transfer System	23-800-1017	FDA UDI	Class I	Unknown
KineMatch® PFR System	22-800-3003	FDA UDI	Class I	Active
KineMatch® PFR System	22-800-1026	FDA UDI	Class I	Unknown
Multi-Directional Tibial Tubercle Transfer System	23-800-1001	FDA UDI	Class I	Active
CarboJet® CO2 Bone Lavage System	25-500-0244	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.