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InMode Ltd.

Medical device makerAI in IsraelAI. FDA records under its name, each linked to the record.

  • 510(k) clearances: 15

Records by Year

Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date

Latest Records

Newest first across sources; each opens the record
DateRecordSource
Jan 15, 2026Ignite RF SystemK251254 · GEI510(k) clearances
Jun 26, 2025Optimas MAX SystemK251632 · GEX510(k) clearances
Nov 14, 2024DEFINE System (AG612444A)K242598 · PBX510(k) clearances
Jul 24, 2024InMode RF SystemK240780 · GEI510(k) clearances
Jun 13, 2024InMode System with the Morpheus8 90 ApplicatorK240017 · GEI510(k) clearances
Mar 20, 2024InMode RF SystemK233642 · GEI510(k) clearances
Oct 13, 2023The Evolve System with the Transform ApplicatorK231495 · GEI510(k) clearances
Jul 20, 2023The InMode System with the Morpheus8 ApplicatorsK231790 · GEI510(k) clearances

Canada and Imports

Matched by company name
Active Health Canada device licences
10, as of Nov 10, 2026
FDA import refusals since 2024
1 shipment lines, through Oct 23, 2026

Names and Identifiers

Appears as
InMode , Ltd.

Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built

Logos are each company's own site icon, matched by name through Wikidata.Company names and logos identify the companies in public FDA and registry records and do not imply endorsement.