Retractable Technologies, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 1
- 510(k) Clearances
- 13
- Inspections
- 5
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|
| Z-1293-2024 | Class II | EasyPoint Needle, 25G x 5/8", REF: 82091 | February 5, 2024 |
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K202325 | EasyPoint Blood Collection Plus | April 9, 2021 |
| K133635 | EASYPOINT NEEDLE | June 17, 2014 |
| K122355 | VANISHPOINT BLOOD COLLECTION SET | August 23, 2013 |
| K112512 | VANISHPOINT BLOOD COLLECTION SET | October 20, 2011 |
| K101708 | PATIENT SAFE LUER CAP | February 24, 2011 |
| K081420 | VANISHPOINT I.V. CATHETER | November 7, 2008 |
| K072654 | PATIENT SAFE SYRINGE | December 14, 2007 |
| K051355 | VANISHPOINT I.V. CATHETER | September 23, 2005 |
| K980069 | VANISHPOINT SYRINGE | February 12, 1998 |
| K973301 | ANTI-STICK SYRINGE WITH INTEGRAL HYPODERMIC NEEDLE/VANISHPOINT SYRINGE | November 7, 1997 |
| K971763 | BLOOD COLLECTION TUBE HOLDER VANISHPOINT TUBE HOLDER/SMALL TUBE ADAPTER | August 26, 1997 |
| K970803 | ANTI-STICK SYRINGE WITH INTEGRAL HYPODERMIC NEEDLE VANISHPOINT SYRINGE | May 29, 1997 |
| K946219 | POP-N-LOK SYRINGE | December 28, 1995 |