Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007682555

FEI Number

3007682555

Entity Name

HOSPITECH RESPIRATION

City/State/Country

Lod Central IL, IL

Establishment Address

1 Galil St., Airport City Industrial Zone, Lod Central IL 701990, IL

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Hospitech Respiration (Owner Number: 10034108)

Owner / Operator Contact Address

1 Galil Str., lod, IL-M 701990, IL

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K131099

PMA Number

N/A

All Registered Proprietary Names

AnapnoGuard ETT AG100S AnapnoGuard MASS MASS

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
BTP	Dropper, Ether	Anesthesiology	Class 1	868.5420	2010-11-05
BSK	Cuff, Tracheal Tube, Inflatable	Anesthesiology	Class 2	868.5750	2018-11-02
KYZ	Syringe, Irrigating (Non Dental)	General Hospital	Class 1	880.6960	2011-01-29
JCX	Apparatus, Suction, Ward Use, Portable, Ac-Powered	General, Plastic Surgery	Class 2	878.4780	2015-01-25

Official Correspondent

No official correspondent registered.

US Agent Details

Tova Rivnay Email: yoram@qsitemed.com Phone: (512) 5354930

Related Public Records

Same Entity

Hospitech Respiration

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

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K082762	Aardvark Medical	AARDVARK NASAL IRRIGATION AND ASPIRATION DEVICE	2008-11-12

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0006-2014	H & H Associates	2	H&H Emergency Cricothyrotomy Kit (Part No. HHECT01/ HHECTK01, NSN 6515-01-573-0692), vacuum sealed and packaged in a 5 mil poly bags, labeled in part *H & H Associates, Inc. CAGE 1NNH6 www.gohandh.com Ordinary, VA 23131 (800) 326-5708*. The product is used to maintain fracture alignment.
Z-0038-05	Kinetic Concepts, Inc	2	V.A.C. X-Large Granufoam Dressing Part Numbers M6275065/5, V.A.C. ATS and V.A.C. Freedom and M6275043/5 V.A.C. Classic. Manufactured by Kinetic Concepts, Inc., San Antonio, Texas 78230

Similar Registrations

Registration Number	Establishment Name	Location
3020831613	KASHI SCIENTIFIC LLC	Portland, OR, US
3018226067	SHANGHAI LONGMANN TECH CO., LTD.	Shanghai, CN
2182318	TIDI PRODUCTS, LLC	NEENAH, WI, US
1056553	REMINGTON MEDICAL, INC.	ALPHARETTA, GA, US
3016438694	ARCH Medical Solutions - Memphis	Lexington, TN, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007682555. Last updated year: 2026. Please use registration number 3007682555 when referencing this establishment in official correspondence.