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 14, 2026, FDA's public records list Vitreq with 16 device recalls and 2 510(k) clearances. The most recent is a 510(k) clearance dated Dec 30, 2020: CryoTreQ.
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.
| Dec 30, 2020 | CryoTreQK202038 · HPS | 510(k) clearances |
| Dec 17, 2019 | VitreQ 23G Pick Needles-REF: CN23.D04 GTIN: 8719214221584Class II · Microscopic tears of the sterile pouch may compromise sterility | Device recalls |
| Dec 17, 2019 | VitreQ 23G Blunt Needles with luer-lock connector-REF: CN23.D05 GTIN: 8719214221621Class II · Microscopic tears of the sterile pouch may compromise sterility | Device recalls |
| Dec 17, 2019 | (1) VitreQ 23G BF Blunt Needles-BF23.D51 GTIN#: 8719214221126 (2) VitreQ 23G BF Brush Needles-BF23.D52 GTIN#: 8719214221140Class II · Microscopic tears of the sterile pouch may compromise sterility | Device recalls |
| Dec 17, 2019 | VitreQ 23G VFI Cannula-REF: CN23.D03 GTIN: 8719214221423Class II · Microscopic tears of the sterile pouch may compromise sterility | Device recalls |
| Dec 17, 2019 | VitreQ 25G VFI Cannula-REF: CN25.D03 GTIN: 8719214221447Class II · Microscopic tears of the sterile pouch may compromise sterility | Device recalls |
| Dec 17, 2019 | VitreQ 20G VFI Cannula-REF: CN20.D03 GTIN: 8719214221485Class II · Microscopic tears of the sterile pouch may compromise sterility | Device recalls |
| Dec 17, 2019 | VitreQ 23G PFC Injection Needle- Ref: MD23.D01 GTIN: 8719214221362Class II · Microscopic tears of the sterile pouch may compromise sterility | Device recalls |
| Dec 17, 2019 | VitreQ 25G Silicone Tipped Cannula-REF: CN25.D01 GTIN: 8719214221522Class II · Microscopic tears of the sterile pouch may compromise sterility | Device recalls |
| May 1, 2019 | Vitreq disposable laser probes, light fibers and ChandelierK182646 · HQB | 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
