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Prosthesis, Larynx (Stents And Keels)
FDA product code FWN · Class 2 · Ear, Nose, Throat
90
Registered devices
9
Adverse events
1
Recalls
10
510(k) clearances
Devices with this code
N/A — BIOMET MICROFIXATION, INCHood Laryngeal Stent — HOOD, E BENSON LABORATORIES INCMehta Laryngeal Stent — HOOD, E BENSON LABORATORIES INCRadiopaque Laryngeal Umbrella Keel — HOOD, E BENSON LABORATORIES INCN/A — BIOMET MICROFIXATION, INCN/A — BIOMET MICROFIXATION, INCN/A — BIOMET MICROFIXATION, INCN/A — BIOMET MICROFIXATION, INCN/A — BIOMET MICROFIXATION, INCRutter Stent — Boston Medical Products, Inc.N/A — BIOMET MICROFIXATION, INCN/A — BIOMET MICROFIXATION, INCRutter Stent — Boston Medical Products, Inc.Mehta Laryngeal Stent — HOOD, E BENSON LABORATORIES INCMontgomery® Laryngeal Keel — Boston Medical Products, Inc.Montgomery® Laryngeal Keel — Boston Medical Products, Inc.Rutter Stent — Boston Medical Products, Inc.Hood Laryngeal Stent — HOOD, E BENSON LABORATORIES INCRutter Stent — Boston Medical Products, Inc.N/A — BIOMET MICROFIXATION, INCMontgomery® Laryngeal Stent — Boston Medical Products, Inc.Rutter Stent — Boston Medical Products, Inc.Laryngeal Umbrella Keel — HOOD, E BENSON LABORATORIES INCN/A — BIOMET MICROFIXATION, INC
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2004-04-22 | Alveolus, Inc. | The tracheal stent may collapse resulting in blockage of the air passage because the stents were not properly coated with the polyurethane material to the very |
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