Simplivia Healthcare , Ltd.
Simplivia Healthcare , Ltd. holds FDA 510(k) medical device clearances, first cleared 2020, most recent 2025, with 1 FDA device recall on record.
Top product codes for Simplivia Healthcare , Ltd.
FDA recalls by Simplivia Healthcare , Ltd.
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 Simplivia Healthcare , Ltd.
- K253033 — Chemfort® 28-day 20 mm Vial Adaptor and 13 mm Convertor
- K251411 — Chemfort Female Luer Lock Adaptor
- K231286 — Chemfort® Catheter Adaptor
- K210707 — OnGuard2 Chemfort Closed Administration (CADM)
- K201142 — TEVADAPTOR Bag Adaptor LL, TEVADAPTOR Bag Adaptor LL with ULTRASITE, TEVADAPTOR Bag Adaptor SP with ULTRASITE, TEVADAPTOR IV Secondary Safety Set with ULTRASITE, TEVADAPTOR IV Secondary Safety set
- K192866 — Chemfort CSTD
Data sourced from openFDA. This site is unofficial and independent of the FDA.