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SprintRay Crown - A3 - Single-unit Capsule 3-Pack

Sprintray, Inc. · Model SRI-0204085 · UDI-DI 00850070544481

EBFEBIELM Prescription
1
510(k) clearances
961
Adverse events (1 deaths)
71
Recalls
207
Facilities

Description

SprintRay Crown is a light-curable polymerizable resin intended to be used for the fabrication of; individual and fixed definitive full single crowns; definitive partial crowns in anterior and posterior area, individual and fixed single veneers; artificial teeth for dental prostheses, which are used for removable definitive full dentures; and individual and removable monolithic full and partial dentures in dental offices and laboratories. The material is an alternative to traditional restorative dental material.

Recalls

DateFirmReason
2026-07-09Henry Schein Inc.Specific lots were distributed in the US with incorrect packaging and Instructions for Use (IFU) from the U.S. FDA-cleared device.
2026-07-09Henry Schein Inc.Specific lots were distributed in the US with incorrect packaging and Instructions for Use (IFU) from the U.S. FDA-cleared device.
2024-08-02Ultradent Products, Inc.Due to a manufacturing issue, red particulates present in the expressed composite.
2024-08-02Ultradent Products, Inc.Due to a manufacturing issue, red particulates present in the expressed composite.
2024-08-02Ultradent Products, Inc.Due to a manufacturing issue, red particulates present in the expressed composite.
2020-08-31Ultradent Products, Inc.Due to a potential manufacturing issue (cross contamination), composite is non-homogeneous.
2019-07-09Voco GmbHThe metal cannula are potentially too loose and may become loose when applying the filing material.
2019-01-31RHONDIUM LIMITEDThe product was mislabeled with an incorrect expiration date.
2017-08-03Ivoclar Vivadent, Inc.Complaints were filed claiming the material consistency was too soft and too sticky in comparison to its usual consistency, causing unexpected handling for the user during packing
2017-08-03Ivoclar Vivadent, Inc.Complaints were filed claiming the material consistency was too soft and too sticky in comparison to its usual consistency, causing unexpected handling for the user during packing

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.