Retractable Technologies, Inc.
Retractable Technologies, Inc. holds FDA 510(k) medical device clearances, first cleared 1995, most recent 2021, with 1 FDA device recall on record.
Top product codes for Retractable Technologies, Inc.
FDA recalls by Retractable Technologies, Inc.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Retractable Technologies, Inc.
- K202325 — EasyPoint Blood Collection Plus
- K133635 — EASYPOINT NEEDLE
- K122355 — VANISHPOINT BLOOD COLLECTION SET
- K112512 — VANISHPOINT BLOOD COLLECTION SET
- K101708 — PATIENT SAFE LUER CAP
- K081420 — VANISHPOINT I.V. CATHETER
- K072654 — PATIENT SAFE SYRINGE
- K051355 — VANISHPOINT I.V. CATHETER
- K980069 — VANISHPOINT SYRINGE
- K973301 — ANTI-STICK SYRINGE WITH INTEGRAL HYPODERMIC NEEDLE/VANISHPOINT SYRINGE
- K971763 — BLOOD COLLECTION TUBE HOLDER VANISHPOINT TUBE HOLDER/SMALL TUBE ADAPTER
- K970803 — ANTI-STICK SYRINGE WITH INTEGRAL HYPODERMIC NEEDLE VANISHPOINT SYRINGE
- K946219 — POP-N-LOK SYRINGE
Data sourced from openFDA. This site is unofficial and independent of the FDA.