Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008274656

FEI Number

3008274656

Entity Name

MOXIMED, INC.

City/State/Country

Fremont, CA, US

Establishment Address

46602 Landing Parkway, Fremont, CA 94538, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Moximed, Inc. (Owner Number: 10031357)

Owner / Operator Contact Address

46602 Landing Parkway, Fremont, CA 94538, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

MISHA(TM) Knee System MISHA(TM) Knee System Torque Limiting Driver MISHA(TM) Knee System Trial MISHA(TM) Knee System Targeting Kit MISHA(TM) Knee System Fixation Kit

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
QVV	Medial Knee Implanted Shock Absorber	Orthopedic	Class 2	888.3610	2023-04-17
HWR	Driver, Prosthesis	Orthopedic	Class 1	888.4540	2023-08-01
HWT	Template	Orthopedic	Class 1	888.4800	2023-08-01
LXH	Orthopedic Manual Surgical Instrument	Orthopedic	Class 1	888.4540	2023-08-01

Official Correspondent

Vijaya Krishnamoorthy

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Moximed, Inc.

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

View Entity Profile →

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.

Similar Registrations

Registration Number	Establishment Name	Location
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2953359	Sterigenics U.S. LLC	Hayward, CA, US
3042969807	INNOORTHO CO., LTD.	Sejong Special Self-Governing City, KR
3015231789	Arthrex Manufacturing Inc.	Pendleton, SC, US
3033509898	STRAITS ORTHOPAEDICS (MFG) SDN BHD	Bandar Cassia Pulau Pinang, MY

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008274656. Last updated year: 2026. Please use registration number 3008274656 when referencing this establishment in official correspondence.