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Ureteral Stent Company

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories1
Latest FDA decision2024-03-22
TypeNumberDevice NameCodeDateActions
510(k) K232920 RELIEF™ Ureteral Stent Kit; Model: RS-001 - 6 Fr x 24cm, RELIEF™ Ureteral Stent Kit; Model: RS-002 - 6 Fr x 26cmFAD2024-03-22 View
510(k) K213444 RELIEF Ureteral Stent Kit; Model: RS-001 - 6 Fr x 24cm, RELIEF Ureteral Stent Kit; Model: RS-002 - 6 Fr x 26cmFAD2022-03-17 View

Related Clinical Trials

NCT06045962Optimal Stent Duration After UreteroscopyACTIVE_NOT_RECRUITINGNCT06719089Evaluation of the Safety and Performance of the Hydrustent® Biodegradable Hydrogel Ureteral StentRECRUITINGNCT06979583Impact of Ureteral Stent and Sheaths Size on Post-Operative PainENROLLING_BY_INVITATIONNCT07535580Patient-Reported Stent Symptom Outcomes and Migration Rates Following Modified Single-J Ureteric Stent Insertion After UreteroscopyCOMPLETEDNCT07580963Stent Related Symptoms Defined by Ureteral Stent Symptom Questionnaire in Patients With Image-Informed Ureteral Stent LengthsNOT_YET_RECRUITINGNCT07627828ComfiJ Versus Conventional Double-J Stent for Ureteral Stent SymptomsRECRUITINGNCT07742358Comparison of Ureteral Stent Designs in Children With Kidney StonesRECRUITING
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