Intersurgical Inc
7 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| One-Piece Guedel Airway, size 00, ISO 5.0, Blue. Oropharyngeal Airway Device. recall (Z-2952-2026) | Intersurgical Inc | 2026-08-14 |
| One-Piece Guedel Airway, size 000, ISO 3.5, Light Green. Oropharyngeal Airway Device. recall (Z-2953-2026) | Intersurgical Inc | 2026-08-14 |
| One-piece Guedel airway, size 2, ISO 8.0, green. Model Number: 1112080. recall (Z-2275-2025) | Intersurgical Inc | 2025-08-06 |
| One-piece Guedel airway, size 3, ISO 9.0, yellow. Model Number: 1113090. recall (Z-2276-2025) | Intersurgical Inc | 2025-08-06 |
| i-view video laryngoscope. Model Number: 8008000. The i-view video laryngoscope is indicat recall (Z-2102-2025) | Intersurgical Inc | 2025-07-11 |
| Intersurgical Solus Standard, laryngeal mask airway, size 3, small adult, 30-50kg Model Nu recall (Z-0096-2023) | Intersurgical Inc | 2022-10-17 |
| The IS Can Disposable CO2 absorber x 6 --- Carbon Dioxide absorbent for use on GE rebreath recall (Z-0518-2012) | Intersurgical Inc | 2012-01-11 |
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Every clearance here is in the API, with alerts when new ones post.