The Total Product Life Cycle (TPLC) database integrates premarket and postmarket data about medical devices. It includes information pulled from CDRH databases including Premarket Approvals (PMA), Premarket Notifications (510[k]), Adverse Events, and Recalls. The TPLC database is refreshed as each of the individual data sources is updated.
The TPLC database description is at http://www.fda.gov/AboutFDA/CentersOffices/CDRH/CDRHTransparency/ucm199906.htm
From this link, the user can move to the search page where you can search the TPLC database by device name, product code (the 3 letter code for each device), or regulation number. The search provides a full report about a particular product line.