Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1220850

FEI Number

1220850

Entity Name

E. Benson Hood Laboratories, Inc.

City/State/Country

Pembroke, MA, US

Establishment Address

575 Washington Street, Pembroke, MA 02359, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Critical Care Diagnostics, Inc (Owner Number: 10059775)

Owner / Operator Contact Address

555 E Eliza St, Schoolcraft, MI 49087, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Hood Laryngeal Stent Hood Y-Stents Various Nasal Splints Hood Tracheal T-Tube Cleaning Kit Hood Nasal Septal Button Dumon Hood Laryngeal Stent Laryngectomy Tube

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FWN	Prosthesis, Larynx (Stents And Keels)	Ear, Nose, Throat	Class 2	874.3620	2026-06-03
NWA	Prosthesis, Tracheal, Preformed/Molded	General, Plastic Surgery	Class 2	878.3720	2026-06-03
EPP	Splint, Nasal	Ear, Nose, Throat	Class 1	874.5800	2026-06-03
BSY	Catheters, Suction, Tracheobronchial	Anesthesiology	Class 1	868.6810	2026-06-03
LFB	Button, Nasal Septal	Unknown	Class U	N/A	2026-06-03
EOQ	Bronchoscope (Flexible Or Rigid)	Ear, Nose, Throat	Class 2	874.4680	2026-06-03
FWN	Prosthesis, Larynx (Stents And Keels)	Ear, Nose, Throat	Class 2	874.3620	2026-06-03
KAC	Tube, Laryngectomy	Ear, Nose, Throat	Class 1	874.4420	2026-06-03

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Critical Care Diagnostics, Inc

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3015489752	C2Dx, Inc.	Schoolcraft, MI, US

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K811059	Pentax Precision Instrument Corp.	PENTAX BRONCHOFIBERSCOPE #FB-15A	1981-05-27
K142934	Covidien	CrossCountry Transbronchial Access Tool straight, CrossCountry Transbronchial Access Tool curved	2015-06-17
K240075	FUJIFILM Healthcare Americas Corporation	FUJIFILM Endoscope Model EB-710XT	2024-02-07

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0025-2020	AURIS HEALTH INC	2	Monarch, Aspirating Biopsy Needle, REF: MBR-000012, Rx Only, UDI: B634MBR0000120

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1220850. Last updated year: 2026. Please use registration number 1220850 when referencing this establishment in official correspondence.