fda
3 records
FDA Recall: Lucid Diagnostics, Inc. — Class II
20240605
The EsophaCap sponge may be at increased risk of detaching from the string during removal of the device from the patient, particularly at the lower es | Product: Brand Name: EsophaCap Product Name: E...
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FDA Device Recall: Brand Name: EsophaCap Product Name: EsophaCap (25mm diameter, 10 pores/inch) M
2024-06-05
Class II — The EsophaCap sponge may be at increased risk of detaching from the string during removal of the device from the patient, particularly at the lower esophageal sphincter at the gastroesophag...
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FDA Device Recall: Brand Name: EsophaCap Product Name: EsophaCap (20mm diameter, 20 pores/inch) M
2024-06-05
Class II — The EsophaCap sponge may be at increased risk of detaching from the string during removal of the device from the patient, particularly at the lower esophageal sphincter at the gastroesophag...
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ny_corps
1 records
NY Corp: LUCID DIAGNOSTICS INC.
2026-05-13
FOREIGN BUSINESS CORPORATION | County: New York | Jurisdiction: Delaware
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SEC EDGAR
1 records
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