FDA data explorer

Every openFDA database, in one search.

30 datasets, 55,850,846 records: approvals, labels, NDCs, shortages, recalls, adverse event reports, device clearances and UDIs, substances, complete response letters and more. openFDA exported the newest on 2026-10-05.

“laser hair removal” matches in 8 of 26 searchable datasets. 18 did not answer this time (Approvals (Drugs@FDA), Orange Book, Drug labels, NDC directory, Drug shortages, Drug recalls, Drug adverse event reports (FAERS), Device classification, PMA approvals, COVID-19 serology test evaluations, Cosmetic adverse event reports, Food recalls, Food and supplement adverse event reports (CAERS), Animal drug adverse event reports, Tobacco product problem reports, UNII codes, NDC SPL data elements, Complete response letters); try again shortly.

Devices

510(k) clearances 37

All 37 in 510(k) clearances →

Establishments and listings 124

All 124 in Establishments and listings →

Device recalls 6

All 6 in Device recalls →

Device recall enforcement reports 6

All 6 in Device recall enforcement reports →

Unique device identifiers (GUDID) 73

  • Venus Velocity · VL000001

    VENUS CONCEPT LTD · The Venus Concept Velocity Diode Laser is intended for all Fitzpatrick skin types, including tanned skin, for use in de…

    DI 07290016540628RxIn Commercial DistributionGEX
    FDA page
  • Diode Laser Hair Removal Machine · GLD01

    Sanhe Meditech Co.Ltd

    DI 06978716980012In Commercial DistributionGEX
    FDA page
  • EXIRA · M126AC1

    EL.EN. SPA · The EXIRA is a medical laser equipped with: - Alexandrite 755 nm laser, that is a high power laser to remove hair and t…

    DI 08057017760979RxIn Commercial DistributionGEX
    FDA page
All 73 in Unique device identifiers (GUDID) →

Device adverse event reports (MAUDE) 37

All 37 in Device adverse event reports (MAUDE) →

Substances & reference

Substances (GSRS) 10

All 10 in Substances (GSRS) →

Historical FDA documents 3

  • FDA NEWS RELEASE FOR IMMEDIATE RELEASE

    FDA NEWS RELEASE FOR IMMEDIATE RELEASE January 16, 2009 FDA Alerts Public about Danger of Skin Numbing Products Serious and life-threatening risks associated with improper use The US. Food and Drug Administration today…

    Press release2 pages
  • NOTE TO CORRESPONDENTS FOR IMMEDIATE RELEASE

    NOTE TO CORRESPONDENTS FOR IMMEDIATE RELEASE Mar. 3, 2009 FDA Consumer Health Information for This Week The U.S. Food and Drug Administration today released its biweekly list of consumer health information updates Updat…

    Press release1 pages
  • FOR IMMEDIATE RELEASE December 5, 2006

    FDA NEWS RELEASE FOR IMMEDIATE RELEASE December 5, 2006 FDA Warns Five Firms To Stop Compounding Topical Anesthetic Creams The Food and Drug Administration (FDA) is warning five firms, Triangle Compounding Pharmacy, Uni…

    Press release2 pages
All 3 in Historical FDA documents →
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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.