--- title: "Post-Market Terms - MedTech Terms" description: "Surveillance, vigilance, recalls, and lifecycle management. 22 vendor-neutral definitions with primary-source citations." lang: en json-ld: | { "@context": "https://schema.org", "@graph": [ { "@type": "DefinedTermSet", "@id": "https://medtechterms.com/categories/post-market#set", "name": "Post-Market - MedTech Terms", "description": "Surveillance, vigilance, recalls, and lifecycle management.", "url": "https://medtechterms.com/categories/post-market", "hasDefinedTerm": [ { "@type": "DefinedTerm", "name": "5-Day Report", "url": "https://medtechterms.com/terms/five-day-report", "termCode": "five-day-report" }, { "@type": "DefinedTerm", "name": "Annual Report (PMA)", "url": "https://medtechterms.com/terms/annual-report-pma", "termCode": "annual-report-pma" }, { "@type": "DefinedTerm", "name": "Customer Notification Letter", "url": "https://medtechterms.com/terms/customer-notification", "termCode": "customer-notification" }, { "@type": "DefinedTerm", "name": "Electronic Medical Device Reporting", "alternateName": "eMDR", "url": "https://medtechterms.com/terms/emdr", "termCode": "emdr" }, { "@type": "DefinedTerm", "name": "FDA Recall Classifications I, II, III", "url": "https://medtechterms.com/terms/recall-classifications", "termCode": "recall-classifications" }, { "@type": "DefinedTerm", "name": "Field Action vs Recall", "url": "https://medtechterms.com/terms/field-action-vs-recall", "termCode": "field-action-vs-recall" }, { "@type": "DefinedTerm", "name": "Field Safety Corrective Action", "alternateName": "FSCA", "url": "https://medtechterms.com/terms/fsca", "termCode": "fsca" }, { "@type": "DefinedTerm", "name": "Global Unique Device Identification Database", "alternateName": "GUDID", "url": "https://medtechterms.com/terms/gudid", "termCode": "gudid" }, { "@type": "DefinedTerm", "name": "Health Hazard Evaluation", "alternateName": "HHE", "url": "https://medtechterms.com/terms/health-hazard-eval", "termCode": "health-hazard-eval" }, { "@type": "DefinedTerm", "name": "Manufacturer Incident Report", "alternateName": "MIR", "url": "https://medtechterms.com/terms/mir", "termCode": "mir" }, { "@type": "DefinedTerm", "name": "Medical Device Recall", "url": "https://medtechterms.com/terms/recall", "termCode": "recall" }, { "@type": "DefinedTerm", "name": "Medical Device Reporting (FDA)", "alternateName": "MDR", "url": "https://medtechterms.com/terms/mdr-reporting", "termCode": "mdr-reporting" }, { "@type": "DefinedTerm", "name": "Medical Device Vigilance", "url": "https://medtechterms.com/terms/vigilance", "termCode": "vigilance" }, { "@type": "DefinedTerm", "name": "Periodic Safety Update Report", "alternateName": "PSUR", "url": "https://medtechterms.com/terms/psur", "termCode": "psur" }, { "@type": "DefinedTerm", "name": "Post-Market Clinical Follow-up", "alternateName": "PMCF", "url": "https://medtechterms.com/terms/pmcf", "termCode": "pmcf" }, { "@type": "DefinedTerm", "name": "Post-Market Performance Follow-up", "alternateName": "PMPF", "url": "https://medtechterms.com/terms/pmpf", "termCode": "pmpf" }, { "@type": "DefinedTerm", "name": "Post-Market Surveillance", "alternateName": "PMS", "url": "https://medtechterms.com/terms/post-market-surveillance", "termCode": "post-market-surveillance" }, { "@type": "DefinedTerm", "name": "Post-Market Surveillance Plan", "url": "https://medtechterms.com/terms/pms-plan", "termCode": "pms-plan" }, { "@type": "DefinedTerm", "name": "PSUR (IVDR Specific)", "url": "https://medtechterms.com/terms/psur-ivdr", "termCode": "psur-ivdr" }, { "@type": "DefinedTerm", "name": "Removal vs Correction (21 CFR 806)", "url": "https://medtechterms.com/terms/removal-vs-correction", "termCode": "removal-vs-correction" }, { "@type": "DefinedTerm", "name": "Section 522 Postmarket Surveillance", "alternateName": "Section 522", "url": "https://medtechterms.com/terms/section-522", "termCode": "section-522" }, { "@type": "DefinedTerm", "name": "Trend Reporting (MDR/MIR)", "url": "https://medtechterms.com/terms/trend-reporting", "termCode": "trend-reporting" } ] }, { "@type": "BreadcrumbList", "itemListElement": [ { "@type": "ListItem", "position": 1, "name": "Home", "item": "https://medtechterms.com/" }, { "@type": "ListItem", "position": 2, "name": "Categories", "item": "https://medtechterms.com/categories" }, { "@type": "ListItem", "position": 3, "name": "Post-Market", "item": "https://medtechterms.com/categories/post-market" } ] } ] } --- [ MedTech Terms The authoritative reference ](/) Browse Learn [Latest](/latest) About [All categories](/categories)Category # Post-Market Surveillance, vigilance, recalls, and lifecycle management. 22 terms [Filter in glossary](/terms?cat=Post-Market) ## Popular post-market terms [ Post-Market Surveillance(PMS) Activities to monitor device safety and performance after market release. ](/terms/post-market-surveillance) ## All Post-Market terms - [5-Day Report ](/terms/five-day-report) - [Annual Report (PMA) ](/terms/annual-report-pma) - [Customer Notification Letter ](/terms/customer-notification) - [Electronic Medical Device Reporting(eMDR) ](/terms/emdr) - [FDA Recall Classifications I, II, III ](/terms/recall-classifications) - [Field Action vs Recall ](/terms/field-action-vs-recall) - [Field Safety Corrective Action(FSCA) ](/terms/fsca) - [Global Unique Device Identification Database(GUDID) ](/terms/gudid) - [Health Hazard Evaluation(HHE) ](/terms/health-hazard-eval) - [Manufacturer Incident Report(MIR) ](/terms/mir) - [Medical Device Recall ](/terms/recall) - [Medical Device Reporting (FDA)(MDR) ](/terms/mdr-reporting) - [Medical Device Vigilance ](/terms/vigilance) - [Periodic Safety Update Report(PSUR) ](/terms/psur) - [Post-Market Clinical Follow-up(PMCF) ](/terms/pmcf) - [Post-Market Performance Follow-up(PMPF) ](/terms/pmpf) - [Post-Market Surveillance(PMS) ](/terms/post-market-surveillance) - [Post-Market Surveillance Plan ](/terms/pms-plan) - [PSUR (IVDR Specific) ](/terms/psur-ivdr) - [Removal vs Correction (21 CFR 806) ](/terms/removal-vs-correction) - [Section 522 Postmarket Surveillance(Section 522) ](/terms/section-522) - [Trend Reporting (MDR/MIR) ](/terms/trend-reporting) ## Explore related categories [Regulatory](/categories/regulatory)[Quality & Risk](/categories/quality-and-risk)[Cybersecurity](/categories/cybersecurity)[Clinical & Trials](/categories/clinical-and-trials)[Standards](/categories/standards)[Software & AI](/categories/software-and-ai)[Manufacturing](/categories/manufacturing)[Investment & Finance](/categories/investment-and-finance)[Market Segments](/categories/market-segments)[Reimbursement](/categories/reimbursement)[Commercialization](/categories/commercialization)[Industry Bodies](/categories/industry-bodies) MedTech Terms An authoritative, plain-language reference for the regulatory, quality, cybersecurity, and software terms that shape modern medical devices. 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