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US
Last updated May 23, 2026
What HOOD, E BENSON LABORATORIES INC makes
The company manufactures single-use and reusable airway management devices, including tracheostomy tubes, nasopharyngeal airways, and various stents for tracheal, bronchial, and nasal applications. Products like the Hood Nasal Septal Button and Reducing Diameter T-Tube are designed for airway support or obstruction relief, while stents such as the Harrell Y Stent and Bronchial Stent with Posts are used in surgical or post-operative settings to maintain patency. Additional items include T-tubes for tracheal bypass and salivary bypass tubes for drainage purposes.
These devices are classified under FDA’s Class I and Class II categories, with some falling under the Unclassified (U) designation, and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates within U.S. regulatory frameworks, ensuring compliance with applicable medical device standards for airway and stenting products.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Hood, E. Benson Laboratories Inc manufacture?
Hood, E. Benson Laboratories Inc specializes in airway management and stenting devices. Their products include tracheostomy tubes (non-reinforced, non-customized, and single-use), nasopharyngeal airways (single-use), and various stents such as tracheal, bronchial, and nasal stents. Examples include the Harrell Y Stent, Bronchial Stent with Posts, and Hood Nasal Septal Button, which are designed for surgical or post-operative airway support, obstruction relief, or patency maintenance.
Where is Hood, E. Benson Laboratories Inc based, and how does this affect its regulatory compliance?
The company is based in the United States, which means its devices are subject to FDA regulatory oversight. Since the devices are listed in the FDA’s Unique Device Identifier (UDI) database, they must comply with U.S. medical device standards and classification rules, including those for airway and stenting products. The FDA categorizes these devices as Class I, Class II, or Unclassified (U), depending on their risk level and intended use.
Which regulatory registries or databases list Hood, E. Benson Laboratories Inc’s devices?
The company’s devices are included in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency in the medical device supply chain, allowing healthcare providers, regulators, and other stakeholders to verify device details such as manufacturer information, model numbers, and classification. Listing in the UDI database is required for compliance with FDA regulations.
How are Hood, E. Benson Laboratories Inc’s devices classified under FDA regulations?
The devices manufactured by Hood, E. Benson Laboratories Inc fall into three classification categories under FDA regulations: Class I (generally low-risk devices), Class II (devices requiring special controls to ensure safety and effectiveness), and Unclassified (U) for those not yet assigned a formal class. Classification depends on factors like the device’s risk level, intended use, and potential impact on patient safety, such as airway obstruction or surgical support.
What is the primary purpose of devices like the Hood Nasal Septal Button or Reducing Diameter T-Tube?
Devices like the Hood Nasal Septal Button are designed to provide support or correct structural issues in the nasal septum, while the Reducing Diameter T-Tube is used in tracheal bypass procedures to maintain airway patency or facilitate drainage. These products are part of a broader range of airway management tools aimed at addressing obstruction, surgical needs, or post-operative care in medical settings.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 076603380
Catalogue (369)
Page 1 of 8| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Harrell Y Stent with Posts | HYPS-14-S | FDA UDI | Class II | Active |
| Bronchial Stent with Posts | BSP-1430-S | FDA UDI | Class II | Active |
| Reducing Diameter T-Tube | HTT-11-8-S | FDA UDI | Class II | Active |
| Hood Nasal Septal Button | NSBT-50-S | FDA UDI | U | Active |
| Tracheal Stent with Rings | TS-1275-S | FDA UDI | Class II | Active |
| Tracheal Stent with Rings | TS-1085-S | FDA UDI | Class II | Active |
| Hood Y Stent | Y-10-S | FDA UDI | Class II | Active |
| Hood Nasal Septal Button | NSB-20-S | FDA UDI | U | Active |
| Tracheal Stent with Rings | TS-2060-S | FDA UDI | Class II | Active |
| Salivary Bypass Tube | SBT-10 | FDA UDI | Class I | Active |
| Radiopaque Standard Tracheal T-Tube | RST-10-S | FDA UDI | Class II | Active |
| Tracheal Stent with Posts | TSP-1890-S | FDA UDI | Class II | Active |
| Huang Inner Ear Shunt | GS-2000 | FDA UDI | Class II | Unknown |
| Radiopaque Bronchial Stent with Posts | RBSP1-1240-S | FDA UDI | Class II | Active |
| Straight Stoma Stent | SS-1530 | FDA UDI | Class II | Active |
| Curved Stoma Stent Set | CS-0213 | FDA UDI | Class II | Active |
| Radiopaque Standard Tracheal T-Tube | RST-14-S | FDA UDI | Class II | Active |
| Angled Stem T-Tube | AST-14-S | FDA UDI | Class II | Active |
| Long Tracheal T-Tube | LT-508-S | FDA UDI | Class II | Active |
| Hood Nasal Septal Button | NSB-30-S | FDA UDI | U | Active |
| Reducing Ends Tracheal Stent with Posts | TSPR-1210-S | FDA UDI | Class II | Active |
| Radiopaque Standard Tracheal T-Tube | RST-11-S | FDA UDI | Class II | Active |
| Hood Y Stent | YM-14-S | FDA UDI | Class II | Active |
| Long Tracheal T-Tube | LT-509-S | FDA UDI | Class II | Unknown |
| Bronchial Stent with Posts | BSP-1040-S | FDA UDI | Class II | Active |
| Westaby T-Y Stent | RTY-10-S | FDA UDI | Class II | Active |
| Tracheal Stent with Mesh and Posts | TSP-1860-M-S | FDA UDI | Class II | Active |
| Esophageal Stent | ESS-14 | FDA UDI | Class I | Active |
| Radiopaque Standard Tracheal T-Tube | RST-15-S | FDA UDI | Class II | Active |
| Salivary Bypass Tube | SBT-08 | FDA UDI | Class I | Active |
| Westaby T-Y Stent | RTY-14-S | FDA UDI | Class II | Active |
| Tracheal Stent with Rings | TS-1075-S | FDA UDI | Class II | Active |
| Ringed T-Tube | RTR-15-S | FDA UDI | Class II | Active |
| Mehta Laryngeal Stent | MLS-10-S | FDA UDI | Class II | Active |
| Bronchial Stent with Rings | BS-0613-S | FDA UDI | Class II | Active |
| Angled Stem T-Tube | AST-12-S | FDA UDI | Class II | Active |
| Long Tracheal T-Tube | LT-509-S | FDA UDI | Class II | Active |
| Long Tracheal T-Tube | LT-512-S | FDA UDI | Class II | Active |
| Pediatric Standard Tracheal T-Tube | ST-507-S | FDA UDI | Class II | Unknown |
| Standard Tracheal T-Tube | ST-515-S | FDA UDI | Class II | Active |
| Y-Stent with Tracheal Posts with 1mm Wall Thickness | YS1-1814-S | FDA UDI | Class II | Active |
| Hood Laryngeal Stent | LSF-25 | FDA UDI | Class II | Active |
| Bronchial Stent with Mesh and Posts | BSP-1230-M-S | FDA UDI | Class II | Active |
| Bronchial Stent with Mesh and Posts | BSP-1440-M-S | FDA UDI | Class II | Active |
| Long Tracheal T-Tube | LT-518-S | FDA UDI | Class II | Unknown |
| Tracheal Stent with Mesh and Posts | TSP-1660-M-S | FDA UDI | Class II | Active |
| Radiopaque Long Tracheal T-Tube | RLT-09-S | FDA UDI | Class II | Active |
| Long Tracheal T-Tube | LT-518-S | FDA UDI | Class II | Active |
| Trachael Stent with Rings | TS-1090-S | FDA UDI | Class II | Active |
| Angled Stem T-Tube | AST-10-S | FDA UDI | Class II | Active |
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