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Hood Laboratories

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Devices
19

What Hood Laboratories makes

Hood Laboratories manufactures devices such as speaking valves, nasal septal buttons, esophageal stents and prostheses, tracheal stoma buttons, bifurcated T-tubes, laryngeal instruments, flexible grasping forceps, acoustic rhinometers, eye valves with scleral buckle, and cleaning kits for tracheal T-tubes.

The company's devices are classified as Class I, Class II, and unclassified (U) and are listed in the FDA 510(k) registry; Hood Laboratories is based in the United States.

AI-generated from registry data, 30 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue19

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  • Hood Speaking Valve Ref K897059

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Hood Nasal Septal Button Ref K920994

    Active Regimes: 510(k) Registry: 510(k) Class:—

  • The Hood Life Saver Ref K853511

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Eliachar Modified Esophageal Stent Ref K904821

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Hood Esophageal Prosthesis Ref K871244

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Acoustic Rhinometer Ref K921452

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Krupin Eye Valve W/Scleral Buckle Ref K885125

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Cleaning Kit Care & Cleaning Of Tracheal T-Tube Ref K853419

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Hood Tracheal Stoma Button Ref K882430

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Hood Bifurcated T-Tube Ref K864533

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Laryngeal Ref K853726

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Flexible Grasping Forceps Ref K854112

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Gibson Endolymphatic Shunt Ref K897049

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Hood Pediatric Tracheostomy Tube Ref K893866

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • The Groningen Voice Prosthesis Ref K853940

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Hood Nasal Splint Ref K890599

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Krupin Eye Valve With Disk Ref K905703

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Hood Tracheal & Tracheal-Bronchial Prostheses Ref K873742

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Silicone Laryngeal Stent Ref K884810

    Active Regimes: 510(k) Registry: 510(k) Class:II

Rows 1-19 of 19

Frequently asked questions

How many devices does Hood Laboratories have in the registry?

The registry currently lists 19 devices for Hood Laboratories. Devices recorded under merged duplicate company entries are counted once.

Which registries list Hood Laboratories's devices?

Among its 19 most recently registered devices, Hood Laboratories has devices listed in FDA 510(k) (19 devices).

What risk classes do Hood Laboratories's devices fall under?

Among its 19 most recently registered devices, the classes recorded for Hood Laboratories's devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Hood Laboratories in the registry?

The most recently registered devices listed for Hood Laboratories include HOOD SPEAKING VALVE, HOOD NASAL SEPTAL BUTTON, THE HOOD LIFE SAVER and ELIACHAR MODIFIED ESOPHAGEAL STENT.

Generated automatically from registry data and not verified by a human reviewer.