It includes information pulled from CDRH databases including Premarket Approvals (PMA), Premarket Notifications (510[k]), Adverse Events, and Recalls. MAUDE data represents reports of adverse events involving medical devices. The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely. The TPLC database is refreshed as each of the individual data sources is updated. Only datasets containing a procode are included in the TPLC database. Although the recall database is updated frequently as items become available, it is merged with the TPLC data on a monthly basis. The TPLC database integrates data by procode, a three-letter code associated with a generic type of medical device. The TPLC reports provide adverse event information as device problem counts based on MAUDE medical device adverse event reports. Submission of the report does not mean the device caused the adverse event.
The .gov means it’s official.Federal government websites often end in .gov or .mil. The TPLC reports include counts of the database information (i.e. The information on this page (the dataset metadata) is also available in these formats. The Premarket Notification database is not updated when 510(k) ownership transfers from the original sponsor to other firm. This database contains a list of classified medical device recalls since November 1, 2002. The TPLC database is refreshed as each of the individual data sources is updated. The TPLC database integrates data by procode, a three-letter code associated with a generic type of medical device. As the various data sources are updated or refreshed, these counts may change. The .gov means it’s official.Federal government websites often end in .gov or .mil. The Total Product Life Cycle (TPLC) database integrates premarket and postmarket data about medical devices. http://www.fda.gov/AboutFDA/CentersOffices/OfficeofMedicalProductsandTob... U.S. Department of Health & Human Services. Before sharing sensitive information, make sure you're on a federal government site. The official HHS motto is "Improving the health, safety, and well-being of America.". As data in MAUDE improves, firm names will become the firm name in the registration database. The Total Product Life Cycle (TPLC) database integrates premarket and postmarket data about medical devices. Adverse events from the MAUDE database cannot be used to determine the rate of adverse events for a particular product or to compare adverse event rates between products. Additional descriptions and disclaimers are available in the table below for each of the data sources. It includes information pulled from CDRH databases including Premarket Approvals (PMA), Premarket Notifications (510[k]), Adverse Events, and Recalls. In addition, adverse events reported via the Alternative Summary Reporting (ASR) Program prior to the program update in 2017 are not included in the MAUDE or TPLC databases. Premarket approval by FDA is the required process of scientific review to ensure the safety and effectiveness of all devices classified as Class III devices. From there, the fund adds its values-based screen. This database is updated on a monthly basis. Applicant/Sponsor/Manufacturer Firm names are not provided with consistent spelling or abbreviations in the MAUDE database. It includes information pulled from CDRH databases including Premarket Approvals (PMA), Premarket Notifications (510[k]), Adverse Events, and Recalls. Details about which events were counted are available through links on the pages. TPLC Factset Analytics Insight TPLC sets its universe by selecting from a parent index of volatility-weighted U.S. large-cap and midcap stocks.
In its current form, the TPLC database provides data by procode, or generic category of device, and not by individual submission or brand name.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely. The site is secure. The data consists of all voluntary reports since June, 1993, user facility reports since 1991, distributor reports since 1993, and manufacturer reports since August, 1996. number of recalls, number of premarket submissions). An official website of the United States government, Recalls, Market Withdrawals and Safety Alerts, CDRH Transparency: Total Product Life Cycle (TPLC), CDRH Transparency: Premarket Submissions, CDRH Transparency: Postmarket Performance and Safety, CDRH Transparency: Compliance & Enforcement, Center for Devices and Radiological Health, Total Product Life Cycle (TPLC) Data Sources and Disclaimers, Alternative Summary Reporting (ASR) Program.
- Washington, D.C. 20201.
Before sharing sensitive information, make sure you're on a federal government site. The United States Department of Health and Human Services (HHS), also known as the Health Department, is a cabinet-level department of the U.S. federal government with the goal of protecting the health of all Americans and providing essential human services. 009:005 - Department of Health and Human Services - Devices and Radiological Health, Open Data Commons Open Database License (ODbL), http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfTPLC/tplc.cfm. You can search the TPLC database by device name or procode to receive a full report about a particular product line. MAUDE data is reported by patients, physicians, facilities and the device manufacturers. You can search the TPLC database by device name or procode to receive a full report about a particular product line. The database is updated monthly. Not all of the entries in the data sources have procodes associated with them, so those data are omitted from the TPLC database. The ASR program ended in June 2019. The Total Product Life Cycle (TPLC) database integrates premarket and postmarket data about medical devices. Only datasets containing a procode are included in the TPLC database. The TPLC database combines data from various CDRH databases (data sources) to present an integrated record of premarket and postmarket activity for medical devices. Preliminary, supplemental and duplicate reports exist. You can search the TPLC database by device name or procode to receive a full report about a particular product line. 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 significantly changed or modified to the extent that its safety or effectiveness could be affected. To aggregate the information all firm names have been simplified and consolidated. Some firm names may not be the current 510(k) owner. Manufacturers submit reports according to their regulatory requirements. An approved Premarket Approval Application (PMA) is, in effect, a private license granted to the applicant for marketing a particular medical device. The site is secure.
In most cases, further investigation is necessary to understand the cause of the adverse event. An official website of the United States government, Recalls, Market Withdrawals and Safety Alerts, CDRH Transparency: Total Product Life Cycle (TPLC), CDRH Transparency: Premarket Submissions, CDRH Transparency: Postmarket Performance and Safety, CDRH Transparency: Compliance & Enforcement, Center for Devices and Radiological Health, Total Product Life Cycle (TPLC) Database Search, Total Product Life Cycle (TPLC) Data Sources and Disclaimers, Contact Us -- Division of Industry and Consumer Education (DICE). https://project-open-data.cio.gov/v1.1/schema, Center for Devices and Radiological Health, U.S. Food and Drug Administration > Center for Devices and Radiological Health, {http://www.fda.gov/AboutFDA/CentersOffices/OfficeofMedicalProductsandTob...}, A federal government website managed by the U.S. Department of Health & Human Services200 Independence Avenue, S.W. The number of reported device problems may not match the number of reports or the number of events, because a report may contain any number of device problem codes and may reference one or more events.