Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 5 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Turbett Surgical with 4 device recalls and 4 510(k) clearances. The most recent is a 510(k) clearance dated Apr 4, 2025: Turbett Surgical Instrument Pod (TS1500); Turbett Surgical Instrument Pod (TS1200); Turb….
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.
| Apr 4, 2025 | Turbett Surgical Instrument Pod (TS1500); Turbett Surgical Instrument Pod (TS1200); Turbett Surgical Instrument Pod (TS1000)K250011 · FRG | 510(k) clearances |
| Apr 1, 2022 | Turbett Surgical Container, TS1500Class II · Eight units manufactured before June 2019 have exhibited weld failures breaching the sterile barrier after prolonged use | Device recalls |
| May 19, 2021 | Turbett Instrument PodK202593 · FRG | 510(k) clearances |
| Apr 30, 2020 | Turbett Instrument PodK200240 · FRG | 510(k) clearances |
| Jan 14, 2016 | Turbett Surgical ContainerK153025 · FRG | 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
