Medical device makerLabelled 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 15, 2026, FDA's public records list Preceptis Medical with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jul 27, 2022: Hummingbird Tympanostomy Tube System.
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.
| Jul 27, 2022 | Hummingbird Tympanostomy Tube SystemK221254 · ETD | 510(k) clearances |
| Jun 5, 2020 | Hummingbird Tympanostomy Tube SystemK200952 · ETD | 510(k) clearances |
| Sep 21, 2015 | Hummingbird Tympanostomy TubeK151830 · ETD | 510(k) clearances |
| Apr 23, 2015 | HUMMINGBIRD(TM) TYMPANOSTOMY TUBE SYSTEM (TTS)K142282 · ETD | 510(k) clearances |
| Aug 22, 2014 | PRECEPTIS TYMPANOSTOMY TUBE INSERTERK133921 · ETD | 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
