Moximed, Inc.
United Statesfrom the FDA registration address FDA FEI 3008274656
- Devices
- 14
- Registrations
- FDA
- FDA recalls
- 11 ongoing
At a glance
Market reach
- United States
- FDA FEI, FDA recalls
Catalogue
Search and filter all 14 devicesCompany details
- FDA FEI number
- 3008274656
- DUNS number
- 808178383
- Address
- 46602 Landing Parkway, Fremont, CA, 94538
FDA recalls
Recalls initiated per year
- 2017 0
- 2018 0
- 2019 0
- 2020 0
- 2021 0
- 2022 0
- 2023 0
- 2024 1
- 2025 0
- 2026 0
2024
- 2 Dec 2024 Z-0762-2025 Class II Ongoing 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, swelling / edema, pain or stiffness, which may necessitate removal of the device.
Frequently asked questions
How many devices does Moximed, Inc. have in the registry?
The registry currently lists 14 devices for Moximed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Moximed, Inc.'s devices?
Among its 14 most recently registered devices, Moximed, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (13 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Moximed, Inc.'s devices fall under?
Among its 14 most recently registered devices, the classes recorded for Moximed, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for Moximed, Inc.?
FDA recall records list 1 recall initiated by Moximed, Inc., the most recent initiated on 2 Dec 2024. 1 of them is recorded as ongoing. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.
What are the newest devices from Moximed, Inc. in the registry?
The most recently registered devices listed for Moximed, Inc. include MISHA® Fixation Kit 2-3001, MISHA® Trial, Large, Right 2-2004, MISHA® Knee System, Small, Right 2-1002 and MISHA® Targeting Kit 2-3002.