About FDA

CDRH Transparency: Total Product Life Cycle (TPLC)

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.

You can search the TPLC database by device name or procode to receive a full report about a particular product line.

In its current form, the TPLC database provides data by procode, or generic category of device, and not by individual submission or brand name.

Page Last Updated: 02/23/2016
Note: If you need help accessing information in different file formats, see Instructions for Downloading Viewers and Players.
Language Assistance Available: Español | 繁體中文 | Tiếng Việt | 한국어 | Tagalog | Русский | العربية | Kreyòl Ayisyen | Français | Polski | Português | Italiano | Deutsch | 日本語 | فارسی | English