Rymed Technologies, LLC
Rymed Technologies, LLC holds FDA 510(k) medical device clearance, cleared in 2017, with 2 FDA device recalls on record.
Top product codes for Rymed Technologies, LLC
FDA recalls by Rymed Technologies, LLC
- Z-0676-2016 — InVision-Plus CS Needleless IV Connector, Catalog Number RYM-7001. Disposable, Single Use. Products are intended for single patient use in intravenous and blood administration sets without the need for needles, thus eliminating the potential for needle-stick injuries during use.
- Z-0675-2016 — InVision-Plus and InVision-Plus Junior Needleless IV Connector, Disposable, Single Use Products are intended for single patient use in intravenous and blood administration sets without the need for needles, thus eliminating the potential for needle-stick injuries during use.
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 Rymed Technologies, LLC
Data sourced from openFDA. This site is unofficial and independent of the FDA.