Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled 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 13, 2026, FDA's public records list Retractable Technologies with 13 510(k) clearances and 1 device recall. The most recent is a device recall dated Feb 5, 2024: EasyPoint Needle, 25G x 5/8", REF: 82091.
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.
| Date | Record | Source |
|---|---|---|
| Feb 5, 2024 | EasyPoint Needle, 25G x 5/8", REF: 82091Class II · The needle cannula of a retractable needle may detach from the needle holder in the patient. | Device recalls |
| Apr 9, 2021 | EasyPoint Blood Collection PlusK202325 · JKA | 510(k) clearances |
| Jun 17, 2014 | EASYPOINT NEEDLEK133635 · FMI | 510(k) clearances |
| Aug 23, 2013 | VANISHPOINT BLOOD COLLECTION SETK122355 · JKA | 510(k) clearances |
| Oct 20, 2011 | VANISHPOINT BLOOD COLLECTION SETK112512 · FPA | 510(k) clearances |
| Feb 24, 2011 | PATIENT SAFE LUER CAPK101708 · FMF | 510(k) clearances |
| Nov 7, 2008 | VANISHPOINT I.V. CATHETERK081420 · FOZ | 510(k) clearances |
| Dec 14, 2007 | PATIENT SAFE SYRINGEK072654 · FMF | 510(k) clearances |
| Sep 23, 2005 | VANISHPOINT I.V. CATHETERK051355 · FOZ | 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
