Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

2027148

FEI Number

2027148

Entity Name

KINAMED, INC.

City/State/Country

CAMARILLO, CA, US

Establishment Address

820 Flynn Rd, CAMARILLO, CA 93012, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

VME ACQUISITION CORP. (Owner Number: 2020352)

Owner / Operator Contact Address

820 FLYNN RD., --, Camarillo, CA 93012, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K964362

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MDM	Instrument, Manual, Surgical, General Use	General, Plastic Surgery	Class 1	878.4800	2013-04-12
GWO	Plate, Cranioplasty, Preformed, Alterable	Neurology	Class 2	882.5320	2013-04-12
GXR	Cover, Burr Hole	Neurology	Class 2	882.5250	2013-04-12
HBW	Fastener, Plate, Cranioplasty	Neurology	Class 2	882.5360	2013-04-12
FQH	Lavage, Jet	General Hospital	Class 2	880.5475	2016-05-25
DZL	Screw, Fixation, Intraosseous	Dental	Class 2	872.4880	2008-03-31
JDQ	Cerclage, Fixation	Orthopedic	Class 2	888.3010	2018-09-05
KTZ	Caliper	Orthopedic	Class 1	888.4150	2014-10-24
FQH	Lavage, Jet	General Hospital	Class 2	880.5475	2008-03-31
JDQ	Cerclage, Fixation	Orthopedic	Class 2	888.3010	2008-03-31
KRR	Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer	Orthopedic	Class 2	888.3540	2008-03-31
LXH	Orthopedic Manual Surgical Instrument	Orthopedic	Class 1	888.4540	2012-12-15
HRS	Plate, Fixation, Bone	Orthopedic	Class 2	888.3030	2008-03-31

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

VME ACQUISITION CORP.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K213616	Becton, Dickinson and Company	BD Surgiphor Antimicrobial Irrigation System	2022-03-23
K874919	Orthomet, Inc.	ORTHOMET WIRE FOR SUTURE, CERCLAGE	1988-01-07
K042598	Zimmer, Inc.	PERIARTICULAR LOCKING PLATES AND SCREWS, 2357 AND 2359 SERIES	2004-10-29
K190842	Jiangsu Trauhui Medical Instrument Co., Ltd.	Comus Locking Plate systems	2020-02-03
K130510	Arthrex, Inc.	ARTHREX COMPRESSION PLATES	2013-09-25

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0009-2007	Smith & Nephew Inc	1	Journey Nonporous Fin-Stem Tibial Punch, Catalog Numbers: 74018811, 74018813, 74018815, 74018817.
Z-0010-2007	Smith & Nephew Inc	1	Genesis II Nonporous Fin-Stem Tibial Punch, Catalog Numbers: 71440480, 71440482, 71440484, 71440486
Z-0011-06	Stryker Howmedica Osteonics Corp.	1	Allocraft TLIF Bone Inserter.
Z-0011-2007	Smith & Nephew Inc	1	Genesis II Oversized Nonporous Fin-Stem Tibial Punch, Catalog Numbers: 71927102, 71927103, 71927104, 71927105
Z-0013-2011	Depuy Orthopaedics, Inc.	1	Summit Broach Handle, NON-STERILE, MFG: DEPUY ORTHOPAEDICS, INC., PO BOX 988 WARSAW, IN 46581, 1 800 366 8143 Catalog Number: 2570-00-000 The Summit Broach Handle (instrumentation) is used with the DePuy Summit Tapered Hip System. The Broach Handle is used to prepare the femur for hip system implantation. The broach handle is an impaction/extraction device that holds broaches for creating the cavity in the femur during hip arthroplasty.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2027148. Last updated year: 2026. Please use registration number 2027148 when referencing this establishment in official correspondence.