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Find a Commonwealth ResourceHealthData.Gov
Federal regulations require that an assembler who installs one or more certified components of a diagnostic x-ray system submit a report of assembly. This database contains the releasable information submitted including…
Updated Oct 29, 2026
HealthData.Gov
This database contains medical device names and associated information developed by the Center. It includes a three letter device product code and a Device Class that refers to the level of CDRH regulation of a given…
Updated Oct 29, 2026
HealthData.Gov
Medical device manufacturers are required to submit a premarket notification or 510(k) if they intend to introduce a device into commercial distribution for the first time or reintroduce a device that will be…
Updated Oct 29, 2026
