co_sos
1 records
fda
18 records
FDA Recall: I.T.S. GmbH — Class II
20260401
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instruct | Product: HCS - Headless Compression Screw Syste...
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FDA Recall: I.T.S. GmbH — Class II
20260401
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instruct | Product: FLS - Foot Locking Plates System and H...
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FDA Recall: I.T.S. GmbH — Class II
20260401
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instruct | Product: Olecranonplate with Angular Stability ...
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FDA Recall: I.T.S. GmbH — Class II
20260401
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instruct | Product: I.T.S. Screw System with the below des...
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FDA Recall: I.T.S. GmbH — Class II
20260401
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instruct | Product: HLS - Hand Locking Plates System with ...
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FDA Recall: I.T.S. GmbH — Class II
20260401
Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instruct | Product: Distal Humeral Plates with Angular Sta...
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FDA Device Recall: HCS - Headless Compression Screw System, Headless Compression Screw, Cannulated;
2026-04-01
Class II — Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
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FDA Device Recall: FLS - Foot Locking Plates System and HOL - Hallux Osteotomy Locking Plate with t
2026-04-01
Class II — Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
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FDA Device Recall: Olecranonplate with Angular Stability with the below descriptions and correspond
2026-04-01
Class II — Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
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FDA Device Recall: I.T.S. Screw System with the below descriptions and corresponding article number
2026-04-01
Class II — Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
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FDA Device Recall: HLS - Hand Locking Plates System with the below descriptions and corresponding a
2026-04-01
Class II — Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
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FDA Device Recall: Distal Humeral Plates with Angular Stability with the below descriptions and cor
2026-04-01
Class II — Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
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FDA Device Recall: I.T.S. Straight Plate with Angular Stability with the below descriptions and cor
2026-04-01
Class II — Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
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FDA Device Recall: Brand Name: I.T.S. Pelvic Reconstruction System (PRS RX & PRS Phoenix) with the
2026-04-01
Class II — Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
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FDA Device Recall: I.T.S. LRS (Locking Reconstruction System) with the below descriptions and corre
2026-04-01
Class II — Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
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FDA Device Recall: I.T.S. Fibula Plate PROlock with Angular Stability with the below descriptions a
2026-04-01
Class II — Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
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FDA Device Recall: Claviculaplate with Angular Stability, with the below descriptions and associate
2026-04-01
Class II — Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
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FDA Device Recall: Rim Plate, 10-Hole, Left, PRS RX System. Titanium, implantable - Product Usage:
2019-06-12
Class II — The titanium implant has the wrong article number laser marked on it.
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nppes
1 records
ny_corps
3 records
NY Corp: ITS PARTNERS LLC
2010-09-27
FOREIGN LIMITED LIABILITY COMPANY | County: Albany | Jurisdiction: Michigan
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NY Corp: I.T.S. HOLDINGS, LLC
2004-06-09
DOMESTIC LIMITED LIABILITY COMPANY | County: New York | Jurisdiction: New York
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NY Corp: ITS ASSOCIATES, LLC
2001-04-05
DOMESTIC LIMITED LIABILITY COMPANY | County: Suffolk | Jurisdiction: New York
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