CourtListener
1 records
Court Opinion: Stimwave Technologies Incorporated v. Laura Tyler Perryman
2022-07-14
Court of Chancery of Delaware | Docket: CA No. 2019-1003-SG | Cited 0x
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fda
8 records
FDA Recall: Stimwave Technologies Inc — Class II
20200909
The product contains a non-functional component not referenced in product labeling. | Product: StimQ Peripheral Nerve Stimulator System (PNS) Models FR4A-SPR-BO US - Product Usage: is used for pe
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FDA Recall: Stimwave Technologies Inc — Class II
20200909
The product contains a non-functional component not referenced in product labeling. | Product: StimQ Peripheral Nerve Stimulator System (PNS) Model FR4A-TRL-AO US - Product Usage: is used for per
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FDA Device Recall: StimQ Peripheral Nerve Stimulator System (PNS) Models FR4A-SPR-BO US - Product U
2020-09-09
Class II — The product contains a non-functional component not referenced in product labeling.
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FDA Device Recall: StimQ Peripheral Nerve Stimulator System (PNS) Model FR4A-TRL-AO US - Product Us
2020-09-09
Class II — The product contains a non-functional component not referenced in product labeling.
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FDA Device Recall: StimQ Peripheral Nerve Stimulator System (PNS) Models: 1. FR4A-RCV-AO US and 2.
2020-09-09
Class II — The product contains a non-functional component not referenced in product labeling.
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FDA Device Recall: StimQ Peripheral Nerve Stimulator System (PNS) Model 1. STQ4-RCV-A0 US and 2.STQ
2020-09-09
Class II — The product contains a non-functional component not referenced in product labeling.
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FDA Device Recall: StimQ Peripheral Nerve Stimulator System (PNS) Models: 1. FR4A-TRL-BO US and 2.
2020-09-09
Class II — The product contains a non-functional component not referenced in product labeling.
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FDA Device Recall: StimQ Peripheral Nerve Stimulator System (PNS) Model STQ4-SPR-BO US - Product Us
2020-09-09
Class II — The product contains a non-functional component not referenced in product labeling.
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