Pacific Instruments is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pacific Instruments - FDA 510(k) Cleared Devices
Recent clearances: Pacific Instruments Orthopedic Fixation Pins and Wires / Kirschner / Guide Wires
1
Total
1
Cleared
0
Denied
Pacific Instruments has 1 FDA 510(k) cleared medical devices. Based in Honolulu, US.
Last cleared in 2022. Active since 2022. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Pacific Instruments Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Novare Medical Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Pacific Instruments
1 devices