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Data / Medical devices / United States / E. Benson Hood Laboratories, Inc.

E. Benson Hood Laboratories, Inc.: FDA-registered device maker in Pembroke, MA, United States, 8 510(k) clearances

E. Benson Hood Laboratories, Inc. is registered with the FDA (registration 1220850) in Pembroke, MA, United States. It lists 11 device types. The FDA files 8 510(k) clearances under its listings, the newest dated January 29, 1999. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
1220850
Address
575 Washington Street, Pembroke, MA, United States, 02359
Owner or operator
Critical Care Diagnostics, Inc (10059775)
Roles
Manufacturer, Repackager or relabeler
First device listed
June 3, 2026
Registered through
2026
Brand names listed
Dumon, Hood Laryngeal Stent, Hood Nasal Septal Button, Hood Stent Introducer, Hood Stoma Stent, Hood T-Tube, Hood Tracheal T-Tube Cleaning Kit, Hood Y-Stents and more

Devices it lists

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
January 29, 1999K983878CZAJA-MCCAFFREY RIGID STENT INTRODUCER/ENDOSCOPEEOQSubstantially EquivalentE. Benson Hood Laboratories, Inc.accessdata.fda.gov
May 15, 1992K920994HOOD NASAL SEPTAL BUTTONLFBSubstantially EquivalentHood Laboratoriesaccessdata.fda.gov
May 10, 1989K884810SILICONE LARYNGEAL STENTFWNSubstantially EquivalentHood Laboratoriesaccessdata.fda.gov
June 28, 1988K882430HOOD TRACHEAL STOMA BUTTONBTOSubstantially EquivalentHood Laboratoriesaccessdata.fda.gov
October 1, 1987K873742HOOD TRACHEAL & TRACHEAL-BRONCHIAL PROSTHESESNWASubstantially EquivalentHood Laboratoriesaccessdata.fda.gov
March 9, 1987K864533HOOD BIFURCATED T-TUBEBTRSubstantially EquivalentHood Laboratoriesaccessdata.fda.gov
March 12, 1986K854414DUMON/HARRELLEOQSubstantially EquivalentBryan Corp.accessdata.fda.gov
May 2, 1984K841347LARYNGEAL STENTFWNSubstantially EquivalentE. Benson Hood Laboratories, Inc.accessdata.fda.gov

Compare with other makers

Updated January 29, 1999. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.