fda
2 records
FDA Device Recall: GentleWave System APM Procedure Instrument with Matrix REF GW-APM-PI02
2022-11-23
Class II — Procedure Instruments with erroneous unit carton labels.
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FDA Device Recall: GentleWave System Posterior CleanFlow Procedure Instrument with Matrices (Single
2022-11-23
Class II — Procedure Instruments with erroneous unit carton labels.
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ny_corps
1 records
NY Corp: SONENDO, INC.
2019-10-22
FOREIGN BUSINESS CORPORATION | County: Albany | Jurisdiction: Delaware
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SEC EDGAR
1 records
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