CFAI
C.F.A.I.
Government Data Intelligence Services

Intersurgical Inc

Company NY
Found in 2 federal databases · 8 total records
fda 7 records
FDA Device Recall: i-view video laryngoscope. Model Number: 8008000. The i-view video laryngosc 2025-07-23
Class I — Potential for faulty devices as a result of depleted batteries.
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FDA Device Recall: Smoothbore breathing system with exhalation port 22 mm Device REF #: B0062001 Cu 2021-01-06
Class II — The device was assembled with the incorrect exhalation port which can cause gas leakage.
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FDA Device Recall: Superset with 22MM ID, Double Swivel Elbow 22MM OD/15MM ID and Bronchoscopy Port 2020-01-15
Class II — The port may crack in the swivel elbow where the flip cap is inserted, and these cracks could possibly leak if they reach a significant size.
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FDA Device Recall: Double Swivel Elbow with Bronchoscopy Port 15MM OD, 22MM OD/15MM ID, REF 1898000 2020-01-15
Class II — The port may crack in the swivel elbow where the flip cap is inserted, and these cracks could possibly leak if they reach a significant size.
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FDA Device Recall: Double Swivel Elbow with Bronchoscopy Port 15MM OD, 22MM OD/15MM ID, REF 1996030 2020-01-15
Class II — The port may crack in the swivel elbow where the flip cap is inserted, and these cracks could possibly leak if they reach a significant size.
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FDA Recall: Intersurgical Inc — Class II 20171213
A defect in the wire-reinforced tubing may result in a partial of total occlusion when the cuff is over-inflated. | Product: Solus Flexible wire-reinforced laryngeal mask airways under the following s...
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FDA Device Recall: Solus Flexible wire-reinforced laryngeal mask airways under the following sizes: 2017-12-13
Class II — A defect in the wire-reinforced tubing may result in a partial of total occlusion when the cuff is over-inflated.
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ny_corps 1 records
NY Corp: INTERSURGICAL INCORPORATED 2023-12-22
FOREIGN BUSINESS CORPORATION | County: Onondaga | Jurisdiction: Indiana
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