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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 1 of 7

Device	Model / Reference	Registries	Class	Status
SuperCable® ISO-Elastic™ Cerclage System	CUSTOM 361	FDA UDI	Class I	Active
SuperCable® ISO-Elastic™ Cerclage System	35-880-1060	FDA UDI	Class I	Active
SuperCable® Grip and Plate System	35-234-5012	FDA UDI	Class II	Active
CarboJet® CO2 Bone Lavage System	25-500-0248	FDA UDI	Class II	Active
SuperCable® Grip and Plate System	35-230-4514	FDA UDI	Class II	Active
NeuroPro®	14-1S3-1635	FDA UDI	Class II	Active
SuperCable® Grip and Plate System	35-840-1020	FDA UDI	Class I	Active
NeuroPro®	14-1T2-0100	FDA UDI	Class I	Active
SuperCable® Grip and Plate System	35-234-5010	FDA UDI	Class II	Active
KineMatch® PFR System	22-800-2004	FDA UDI	Class I	Active
SuperCable® Grip and Plate System	35-230-4522	FDA UDI	Class II	Active
NeuroPro®	14-1DY-1605	FDA UDI	Class I	Active
SuperCable® Grip and Plate System	35-234-5028	FDA UDI	Class II	Active
MD3T™ Multi-Directional Tibial Tubercle Transfer System	23-800-2013	FDA UDI	Class I	Active
NeuroPro®	14-1P1-0812	FDA UDI	Class II	Active
NeuroPro® Low Profile	16-1S1-2006	FDA UDI	Class II	Active
NeuroPro® Low Profile	16-1T1-0610	FDA UDI	Class I	Active
SuperCable® ISO-Elastic™ Cerclage System	35-800-3120	FDA UDI	Class I	Active
KineMatch® PFR System	22-800-3001	FDA UDI	Class I	Active
KineMatch® PFR System	22-800-1024	FDA UDI	Class I	Unknown
NeuroPro® Low Profile	16-1P1-1480	FDA UDI	Class II	Active
NeuroPro® Low Profile	16-1S3-1644	FDA UDI	Class II	Active
SuperCable® ISO-Elastic™ Cerclage System	35-800-3102	FDA UDI	Class I	Active
SuperCable® Grip and Plate System	35-860-2065	FDA UDI	Class II	Active
SuperCable® Grip and Plate System	35-230-4534	FDA UDI	Class II	Active
MD3T™ Multi-Directional Tibial Tubercle Transfer System	23-800-2070	FDA UDI	Class I	Unknown
SuperCable® Grip and Plate System	35-230-4538	FDA UDI	Class II	Active
NeuroPro® Low Profile	16-1P1-0211	FDA UDI	Class II	Active
SuperCable® Grip and Plate System	35-230-4530	FDA UDI	Class II	Active
SuperCable® Grip and Plate System	35-860-1070	FDA UDI	Class I	Active
NeuroPro®	14-1S1-1605	FDA UDI	Class II	Active
NeuroPro® Low Profile	16-1P2-0218	FDA UDI	Class II	Active
NeuroPro®	14-1T1-0158	FDA UDI	Class I	Active
NeuroPro®	14-1DP-1604	FDA UDI	Class I	Active
NeuroPro® Low Profile	16-1P3-3867	FDA UDI	Class II	Active
SuperCable® ISO-Elastic™ Cerclage System	35-800-2020	FDA UDI	Class I	Active
SuperCable® Grip and Plate System	35-230-4550	FDA UDI	Class II	Active
CarboJet® CO2 Bone Lavage System	25-200-0130	FDA UDI	Class II	Active
Multi-Directional Tibial Tubercle Transfer System	23-800-1003	FDA UDI	Class I	Active
KineMatch® PFR System	20-420-0104	FDA UDI	Class II	Active
SuperCable® ISO-Elastic™ Cerclage System	38-800-3400	FDA UDI	Class I	Active
NeuroPro®	14-1S2-1604	FDA UDI	Class II	Active
SuperCable® ISO-Elastic™ Cerclage System	35-880-2060	FDA UDI	Class I	Active
Multi-Directional Tibial Tubercle Transfer System	23-800-1011	FDA UDI	Class I	Active
SuperCable® ISO-Elastic™ Cerclage System	35-400-3010	FDA UDI	Class II	Active
NeuroPro®	14-1P1-0413	FDA UDI	Class II	Active
CarboJet® CO2 Bone Lavage System	25-200-0232	FDA UDI	Class II	Active
Multi-Directional Tibial Tubercle Transfer System	23-800-1025	FDA UDI	Class I	Unknown
NeuroPro® Low Profile	16-1S3-1605	FDA UDI	Class II	Active
SuperCable® ISO-Elastic™ Cerclage System	CUSTOM 370	FDA UDI	Class I	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.