Facility

MOXIMED, INC.

1 recall(s) on record — most severe on record: Class II.

Key facts

1recalls · worst Class II

2inspections · worst VAI

—warning letters in our data

Recalls are listed for the parent company: openFDA recall records do not name a facility. How we attribute records

FDA Establishment Identifier (FEI)	3008274656
Establishment type	Manufacture Medical Device
Location	46602 Landing Parkway Fremont, CA, US 94538
Registration status	Active · expires 2026
Parent company	Moximed, Inc. (owner-operator 10031357)
Brand names	MISHA(TM) Knee System Trial; MISHA(TM) Knee System Targeting Kit

Activity by year

Recalls (1)
Inspections (2)

Devices registered here (1)

Template
Product code HWT (opens in a new tab) · Class I · Orthopedic · 21 CFR 888.4800

Recalls & enforcement

Class IIOngoing2024-12-02
Knee implant may fracture due to a supplier-related issue with one component that has nonconforming geometry at the distal end of the absorber component that may result in a reduced wall thickness and microcracks, which may lead to new or worsening symptoms of discomfort, swellin…

FDA inspections (2)

NAI2025-10-28
No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices
VAI2017-07-07
Voluntary Action Indicated · Bioresearch Monitoring · citations posted

Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.

All facilities operated by Moximed, Inc.

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “MOXIMED, INC. (FEI 3008274656) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3008274656-moximed-inc/

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