FirmLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Geon Corporation with 5 510(k) clearances. The most recent is a 510(k) clearance dated Feb 4, 2025: Geon (S2) Nasal Aspirator.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Feb 4, 2025 | Geon (S2) Nasal AspiratorK243138 · BTA | 510(k) clearances |
| Feb 2, 2023 | Geonic Nasal Aspirator, Geonic Nasal CleanerK220126 · BTA | 510(k) clearances |
| Jun 2, 2010 | GEON RAPID DIGITAL THERMOMETER MODEL: MT-B117, MT-B127, MT-B130, MT-B132FAK100563 · FLL | 510(k) clearances |
| Jan 12, 2001 | GEON DIGITAL CLINICAL THERMOMETERK003223 · FLL | 510(k) clearances |
| Oct 18, 1996 | GEON ELECTRONIC THERMOMETERK952001 · FLL | 510(k) clearances |
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
