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APEX Base - Opaque Original Pink - 3kg

Sprintray, Inc. · Model SRI-0202194 · UDI-DI 00850070544443

EBI Prescription
1
510(k) clearances
178
Adverse events
16
Recalls
172
Facilities

Description

SprintRay Apex Base resin is a light-curable polymerizable resin intended to be used for the fabrication and repair of full and partial removable dentures and baseplates. The material is an alternative to traditional denture base material.

Recalls

DateFirmReason
2024-01-19STRATASYS LTDCustomers unable to use cartridges due to formatting error in expiration date which leads to switching the day with the month. Or, the system will not recognize that a resin is exp
2024-01-19STRATASYS LTDCustomers unable to use cartridges due to formatting error in expiration date which leads to switching the day with the month. Or, the system will not recognize that a resin is exp
2024-01-19STRATASYS LTDCustomers unable to use cartridges due to formatting error in expiration date which leads to switching the day with the month. Or, the system will not recognize that a resin is exp
2024-01-19STRATASYS LTDCustomers unable to use cartridges due to formatting error in expiration date which leads to switching the day with the month. Or, the system will not recognize that a resin is exp
2024-01-19STRATASYS LTDCustomers unable to use cartridges due to formatting error in expiration date which leads to switching the day with the month. Or, the system will not recognize that a resin is exp
2023-10-24GRAPHENANO DENTAL SLMachining error on cams renders the device unusable.
2023-04-10Keystone IndustriesThe Hard Line Chairside Reline Kit (570-0718) (0921940HS) was labeled as Soft Line Chairside Reline Kit (570-0717) (0921250HS) on the outer box. The contents of the Kit and the IFU
2022-01-06Envisiontec US LlcManufactured in a non-FDA-registered manufacturing facility and product mislabeled as being of German origin
2022-01-06Envisiontec US LlcManufactured in a non-FDA-registered manufacturing facility and product mislabeled as being of German origin
2018-09-12CMP Industries, LlcForeign material in product

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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.