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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 5 of 7

Device	Model / Reference	Registries	Class	Status
KineMatch® PFR System	22-800-2002	FDA UDI	Class I	Active
NeuroPro® Low Profile	16-1S1-1605	FDA UDI	Class II	Active
SuperCable® ISO-Elastic™ Cerclage System	35-800-2000	FDA UDI	Class I	Active
MD3T™ Multi-Directional Tibial Tubercle Transfer System	23-800-4030	FDA UDI	Class I	Active
NeuroPro®	14-1DA-X605	FDA UDI	Class I	Active
NeuroPro®	14-1P3-8613	FDA UDI	Class II	Active
NeuroPro®	14-1P3-0886	FDA UDI	Class II	Active
KineMatch® PFR System	22-800-1020	FDA UDI	Class I	Active
CarboJet® CO2 Bone Lavage System	25-200-0152	FDA UDI	Class II	Active
MD3T™ Multi-Directional Tibial Tubercle Transfer System	23-800-1027	FDA UDI	Class I	Unknown
Multi-Directional Tibial Tubercle Transfer System	23-800-1029	FDA UDI	Class I	Active
NeuroPro®	14-1S1-1604	FDA UDI	Class II	Active
MD3T™ Multi-Directional Tibial Tubercle Transfer System	23-800-1032	FDA UDI	Class I	Active
SuperCable® Grip and Plate System	35-860-2060	FDA UDI	Class I	Active
NeuroPro® Low Profile	16-1P1-0810	FDA UDI	Class II	Active
SuperCable® ISO-Elastic™ Cerclage System	35-400-2005	FDA UDI	Class II	Active
SuperCable® Grip and Plate System	35-220-1010	FDA UDI	Class II	Active
NeuroPro®	14-1P3-9013	FDA UDI	Class II	Active
KineMatch® PFR System	Custom 104	FDA UDI	Class I	Active
SuperCable® Grip and Plate System	35-234-5036	FDA UDI	Class II	Active
CarboJet® CO2 Bone Lavage System	25-200-0160	FDA UDI	Class II	Active
KineMatch® PFR System	Custom 266	FDA UDI	Class I	Active
NeuroPro®	14-1P2-0318	FDA UDI	Class II	Active
NeuroPro® Low Profile	16-1T1-0300	FDA UDI	Class I	Active
NeuroPro®	14-1DA-1605	FDA UDI	Class I	Active
KineMatch® PFR System	22-800-3022	FDA UDI	Class I	Active
KineMatch® PFR System	20-420-0103	FDA UDI	Class II	Active
KineMatch® PFR System	22-800-3024	FDA UDI	Class I	Active
KineMatch® PFR System	22-800-4003	FDA UDI	Class I	Active
NeuroPro®	14-1T1-0300	FDA UDI	Class I	Active
NeuroPro®	14-1P1-1277	FDA UDI	Class II	Active
KineMatch® PFR System	22-800-3026	FDA UDI	Class I	Active
NeuroPro®	14-1P3-8622	FDA UDI	Class II	Active
SuperCable® ISO-Elastic™ Cerclage System	35-800-3250	FDA UDI	Class I	Active
SuperCable® ISO-Elastic™ Cerclage System	35-880-1040	FDA UDI	Class I	Active
SuperCable® Grip and Plate System	35-860-1020	FDA UDI	Class II	Active
NeuroPro®	14-1T1-0340	FDA UDI	Class I	Unknown
SuperCable® ISO-Elastic™ Cerclage System	35-800-2100	FDA UDI	Class I	Active
NeuroPro®	14-1P1-1266	FDA UDI	Class II	Active
SuperCable® Grip and Plate System	35-800-4030	FDA UDI	Class I	Active
NeuroPro®	14-1S3-1605	FDA UDI	Class II	Active
CarboJet® CO2 Bone Lavage System	25-200-0140	FDA UDI	Class II	Active
NeuroPro®	14-1DG-X605	FDA UDI	Class I	Active
SuperCable® ISO-Elastic™ Cerclage System	35-800-3002	FDA UDI	Class I	Active
KineMatch® PFR System	22-800-3021	FDA UDI	Class I	Active
SuperCable® Grip and Plate System	35-860-3020	FDA UDI	Class I	Unknown
Multi-Directional Tibial Tubercle Transfer System	23-800-1013	FDA UDI	Class I	Active
NeuroPro®	14-1DP-1605	FDA UDI	Class I	Active
SuperCable® Grip and Plate System	35-230-4540	FDA UDI	Class II	Active
KineMatch® PFR System	22-100-1001	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.