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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 3 of 7

Device	Model / Reference	Registries	Class	Status
MD3T™ Multi-Directional Tibial Tubercle Transfer System	23-800-2011	FDA UDI	Class I	Active
SuperCable® Grip and Plate System	35-234-5050	FDA UDI	Class II	Active
SuperCable® Grip and Plate System	35-234-5038	FDA UDI	Class II	Active
KineMatch® PFR System	22-800-4004	FDA UDI	Class I	Active
CarboJet® CO2 Bone Lavage System	25-300-1010	FDA UDI	Class I	Active
SuperCable® Iso-Elastic™ Cerclage System	35-100-1040	FDA UDI	Class II	Active
KineMatch® PFR System	22-800-2007	FDA UDI	Class I	Active
NeuroPro® Low Profile	16-1P2-0125	FDA UDI	Class II	Active
SuperCable® Grip and Plate System	35-230-4528	FDA UDI	Class II	Active
MD3T™ Multi-Directional Tibial Tubercle Transfer System	23-800-4520	FDA UDI	Class I	Active
SuperCable® Grip and Plate System	35-234-5032	FDA UDI	Class II	Active
NeuroPro®	14-1S2-1606	FDA UDI	Class II	Active
CarboJet® CO2 Bone Lavage System	25-200-0242	FDA UDI	Class II	Active
KineMatch® PFR System	Custom 260	FDA UDI	Class I	Active
SuperCable® Grip and Plate System	35-850-1010	FDA UDI	Class I	Active
CarboJet XF® Bone Preparation System	27-100-1140	FDA UDI	Class II	Active
SuperCable® Grip and Plate System	35-234-5034	FDA UDI	Class II	Active
MD3T™ Multi-Directional Tibial Tubercle Transfer System	23-800-1018	FDA UDI	Class I	Active
SuperCable® Grip and Plate System	35-220-2010	FDA UDI	Class II	Active
KineMatch® PFR System	22-800-3027	FDA UDI	Class I	Active
NeuroPro®	14-1T1-0510	FDA UDI	Class I	Unknown
NeuroPro®	14-1S4-1604	FDA UDI	Class II	Active
KineMatch® PFR System	22-800-2010	FDA UDI	Class I	Active
SuperCable® ISO-Elastic™ Cerclage System	35-800-6000	FDA UDI	Class I	Unknown
CarboJet XF® Bone Preparation System	27-100-1010	FDA UDI	Class II	Active
SuperCable® Grip and Plate System	35-234-5016	FDA UDI	Class II	Active
NeuroPro® Low Profile	16-1S1-1635	FDA UDI	Class II	Active
NeuroPro® Low Profile	16-1P2-0318	FDA UDI	Class II	Active
SuperCable® ISO-Elastic™ Cerclage System	35-800-1001	FDA UDI	Class I	Unknown
SuperCable® ISO-Elastic™ Cerclage System	35-800-3000	FDA UDI	Class I	Active
SuperCable® Grip and Plate System	35-860-2062	FDA UDI	Class I	Active
SuperCable® Grip and Plate System	35-234-5026	FDA UDI	Class II	Active
CarboJet® CO2 Bone Lavage System	25-200-0270	FDA UDI	Class II	Active
NeuroPro®	14-1P3-9020	FDA UDI	Class II	Active
SuperCable® Grip and Plate System	35-860-2030	FDA UDI	Class II	Active
SuperCable® Grip and Plate System	35-234-5040	FDA UDI	Class II	Active
NeuroPro®	14-1T1-0610	FDA UDI	Class I	Active
SuperCable® ISO-Elastic™ Cerclage System	35-800-3300	FDA UDI	Class I	Active
NeuroPro® Low Profile	16-1P3-3869	FDA UDI	Class II	Active
MD3T™ Multi-Directional Tibial Tubercle Transfer System	23-800-1026	FDA UDI	Class I	Active
SuperCable® Grip and Plate System	35-860-2070	FDA UDI	Class I	Active
NeuroPro® Low Profile	16-1P1-0413	FDA UDI	Class II	Active
NeuroPro®	14-1S2-2005	FDA UDI	Class II	Active
NeuroPro®	14-1P3-8615	FDA UDI	Class II	Active
MD3T™ Multi-Directional Tibial Tubercle Transfer System	23-800-1015	FDA UDI	Class I	Active
NeuroPro® Low Profile	16-1S1-2005	FDA UDI	Class II	Active
CarboJet® CO2 Bone Lavage System	25-400-1000	FDA UDI	Class I	Active
NeuroPro® Low Profile	16-1P3-8913	FDA UDI	Class II	Active
CarboJet® CO2 Bone Lavage System	25-200-0230	FDA UDI	Class II	Active
NeuroPro® Low Profile	16-1S3-1604	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.