# E. Benson Hood Laboratories, Inc. (manufacturer, Pembroke, MA): 13 new FDA device listings, incl. bronchoscope (flexible or rigid)

**Score:** 85/100

| Field | Value |
|---|---|
| Establishment | E. Benson Hood Laboratories, Inc. |
| Owner / operator | Critical Care Diagnostics, Inc |
| Role | Manufacturer |
| Establishment types | Repack or Relabel Medical Device; Manufacture Medical Device |
| Location | Pembroke, MA, US |
| New listings | 13 |
| Devices | Bronchoscope (Flexible Or Rigid); Tube, Laryngectomy; Cannula, Sinus; Prosthesis, Larynx (Stents And Keels); Button, Nasal Septal; Tube, Tracheal (W/Wo Connector); Tube, Tracheostomy (W/Wo Connector); Splint, Nasal; Prosthesis, Tracheal, Preformed/Molded; Catheters, Suction, Tracheobronchial |
| Product codes | EOQ, KAC, KAM, FWN, LFB, BTR, BTO, EPP, NWA, BSY, CBH |
| Device classes | Class I, Class II, Unclassified |
| Medical specialties | Ear, Nose, Throat, General, Plastic Surgery, Anesthesiology |
| Brand names | Hood Stent Introducer; Laryngectomy Tube; Jacobs Sinus Cannula; Hood Laryngeal Stent; Hood Nasal Septal Button; Dumon; Hood T-Tube; Hood Stoma Stent |
| First new listing | 2026-06-03 |
| Latest new listing | 2026-06-03 |
| FDA registration number | 1220850 |
| Registration expires | 2026-12-31 |

## Why this score
- Brings its own devices to market: buys manufacturing, sterilization and QMS help.
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.
- U.S. establishment.

Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) (https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm). Last refreshed: 2026-10-28T20:51:27.468Z.
From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.