FDA data explorer

Every openFDA database, in one search.

30 datasets, 55,847,670 records: approvals, labels, NDCs, shortages, recalls, adverse event reports, device clearances and UDIs, substances, complete response letters and more. openFDA exported the newest on 2026-09-26.

“exosome” matches in 4 of 26 searchable datasets. 22 did not answer this time (Approvals (Drugs@FDA), Orange Book, Drug labels, NDC directory, Drug shortages, Drug recalls, Device classification, 510(k) clearances, PMA approvals, Device recalls, Device recall enforcement reports, Device adverse event reports (MAUDE), COVID-19 serology test evaluations, Food recalls, Food and supplement adverse event reports (CAERS), Animal drug adverse event reports, Tobacco product problem reports, Substances (GSRS), UNII codes, NDC SPL data elements, Historical FDA documents, Complete response letters); try again shortly.

Drugs

Drug adverse event reports (FAERS) 27

  • Injection site pain, Erythema, Scab +7

    Drugs: UNAPPROVED DRUG COSMETIC PRODUCTS, STEM CELL, EXOSOME, GROWTH FACTOR OR TISSUE DERIVED UNAPPROVED PRODUCT, ZYRTEC +5

    SeriousDisabilityReport 26884216
  • Application site mass, Product use issue

    Drugs: STEM CELL, EXOSOME, GROWTH FACTOR OR TISSUE DERIVED UNAPPROVED PRODUCT, Womens Daily Multivitamin, OMEGA 3

    SeriousOther seriousReport 26554917
  • Off label use, Hypoaesthesia

    Drugs: STEM CELL, EXOSOME, GROWTH FACTOR OR TISSUE DERIVED UNAPPROVED PRODUCT, ZINC, VITAMIN C +1

    Not seriousReport 26485908
All 27 in Drug adverse event reports (FAERS) →

Devices

Establishments and listings 6

All 6 in Establishments and listings →

Cosmetics

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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.