Rymed Technologies, LLC

FDA Regulatory Profile

Rymed Technologies, LLC appears in FDA public data with 2 recalls, 4 510(k) clearances, 3 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-0676-2016, Class II) was initiated on January 5, 2016. Its most recent 510(k) clearance was granted on June 15, 2017.

Summary

Total Recalls
2
510(k) Clearances
4
Inspections
3
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-0676-2016Class IIInVision-Plus CS Needleless IV Connector, Catalog Number RYM-7001. Disposable, Single Use. ProdJanuary 5, 2016
Z-0675-2016Class IIInVision-Plus and InVision-Plus Junior Needleless IV Connector, Disposable, Single Use Products aJanuary 5, 2016

Recent 510(k) Clearances

K-NumberDeviceDate
K162826Encore NeutralJune 15, 2017
K093489IN VISION-PLUS NANO WITH NEUTRAL ADVANTAGE TECHNOLOGYJuly 29, 2010
K991653INVISION-PLUS INJECTION PORT CONNECTOR SYSTEMJune 24, 1999
K960771SLAV AND SLAV-ONE INJECTION PORT CONNECTOR SYSTEMDecember 10, 1996