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GC RELINE™ II

Gc America Inc. · Model 010261 · UDI-DI 14548161321372

EBI Prescription
1
510(k) clearances
179
Adverse events
16
Recalls
173
Facilities

Description

GC RELINE™ II Intro Kit ExtraSoft contains: 1 GC RELINE II Cartridge ExtraSoft 57g (48mL), 1 GC RELINE II Primer for Resin 8g (10mL), 1 GC RELINE II Point for Trimming, 1 GC RELINE II Wheel for Finishing, 1 GC RELINE II Remover for Resin 5g(5.5mL), 6 pieces Mixing Tip II L, 3 disposable brushes, 1 plastic spatula

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.