Medical Device Manufacturer · US , San Diego , CA

Eisertech, LLC - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 2011

Recent clearances: Temporary Fixation Pins, Cervical Plate

Total

Cleared

Denied

Eisertech, LLC has 8 FDA 510(k) cleared medical devices. Based in San Diego, US.

Historical record: 8 cleared submissions from 2011 to 2019. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Eisertech, LLC Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Mrc-X, LLC as regulatory consultant.

Eisertech, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Eisertech, LLC

8 devices

1-8 of 8

Cleared Dec 26, 2019

Temporary Fixation Pins

Eisertech, LLC - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Eisertech, LLC

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