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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 2 of 7

Device	Model / Reference	Registries	Class	Status
CarboJet® CO2 Bone Lavage System	25-200-0200	FDA UDI	Class II	Active
SuperCable® ISO-Elastic™ Cerclage System	35-800-2120	FDA UDI	Class I	Active
SuperCable® ISO-Elastic™ Cerclage System	35-800-5000	FDA UDI	Class I	Unknown
SuperCable® Grip and Plate System	35-200-1030	FDA UDI	Class II	Active
MD3T™ Multi-Directional Tibial Tubercle Transfer System	23-800-1023	FDA UDI	Class I	Unknown
SuperCable® ISO-Elastic™ Cerclage System	35-800-3020	FDA UDI	Class I	Active
SuperCable® ISO-Elastic™ Cerclage System	35-800-3302	FDA UDI	Class I	Active
NeuroPro®	14-1P2-0218	FDA UDI	Class II	Active
CarboJet® CO2 Bone Lavage System	25-100-2001	FDA UDI	Class II	Active
NeuroPro® Low Profile	16-1P1-3184	FDA UDI	Class II	Active
NeuroPro®	14-1T1-0620	FDA UDI	Class I	Active
SuperCable® Grip and Plate System	35-220-3010	FDA UDI	Class II	Active
NeuroPro®	14-1T1-0500	FDA UDI	Class I	Active
SuperCable® Grip and Plate System	35-230-4524	FDA UDI	Class II	Active
NeuroPro® Low Profile	16-1T1-0410	FDA UDI	Class I	Active
SuperCable® Grip and Plate System	35-860-2082	FDA UDI	Class I	Active
NeuroPro®	14-1T1-0240	FDA UDI	Class I	Active
NeuroPro®	14-1DK-1605	FDA UDI	Class I	Active
CarboJet® CO2 Bone Lavage System	25-200-0150	FDA UDI	Class II	Active
SuperCable® Grip and Plate System	35-860-2020	FDA UDI	Class II	Active
NeuroPro®	14-1DH-1605	FDA UDI	Class I	Active
SuperCable® ISO-Elastic™ Cerclage System	35-800-7000	FDA UDI	Class I	Active
SuperCable® Grip and Plate System	35-220-2012	FDA UDI	Class II	Active
NeuroPro®	14-1S2-1605	FDA UDI	Class II	Active
NeuroPro®	14-1S3-1604	FDA UDI	Class II	Active
NeuroPro® Low Profile	16-1S1-1606	FDA UDI	Class II	Active
KineMatch® PFR System	22-800-2011	FDA UDI	Class I	Active
NeuroPro®	14-1S2-1635	FDA UDI	Class II	Active
NeuroPro®	14-1P1-0810	FDA UDI	Class II	Active
CarboJet® CO2 Bone Lavage System	25-200-0220	FDA UDI	Class II	Active
NeuroPro®	14-1P1-0612	FDA UDI	Class II	Active
KineMatch® PFR System	22-800-3005	FDA UDI	Class I	Active
KineMatch® PFR System	22-100-1002	FDA UDI	Class II	Active
NeuroPro® Low Profile	16-1P1-0612	FDA UDI	Class II	Active
SuperCable® Iso-Elastic™ Cerclage System	35-400-1010	FDA UDI	Class I	Unknown
NeuroPro® Low Profile	16-1T1-0600	FDA UDI	Class I	Active
NeuroPro® Low Profile	16-1P1-0214	FDA UDI	Class II	Active
SuperCable® Grip and Plate System	35-234-5024	FDA UDI	Class II	Active
Multi-Directional Tibial Tubercle Transfer System	23-800-1005	FDA UDI	Class I	Active
SuperCable® ISO-Elastic™ Cerclage System	35-800-2050	FDA UDI	Class I	Unknown
NeuroPro®	14-1T1-0400	FDA UDI	Class I	Active
SuperCable® Grip and Plate System	35-860-2080	FDA UDI	Class I	Active
CarboJet® CO2 Bone Lavage System	25-200-0246	FDA UDI	Class II	Active
CarboJet® CO2 Bone Lavage System	25-200-0300	FDA UDI	Class I	Active
SuperCable® Grip and Plate System	35-230-4512	FDA UDI	Class II	Active
SuperCable® ISO-Elastic™ Cerclage System	CUSTOM 371	FDA UDI	Class I	Active
CarboJet® CO2 Bone Lavage System	25-200-0100	FDA UDI	Class II	Active
NeuroPro®	14-1P3-8620	FDA UDI	Class II	Active
KineMatch® PFR System	22-800-3017	FDA UDI	Class I	Active
Multi-Directional Tibial Tubercle Transfer System	23-800-1019	FDA UDI	Class I	Unknown

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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.