United States Endoscopy Group, Inc.
Active in EUDAMEDUnited Statesfrom SRN EUDAMED FDA SRN US-MF-000017968 FEI 1000122656
- Devices
- 96
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
At a glance
Market reach
- European Union
- EUDAMED actor
- United States
- FDA FEI
What United States Endoscopy Group, Inc. makes
United States Endoscopy Group, Inc. manufactures endoscopic accessories and procedural devices, including pull PEG kits, guidewire PEG kits, concentric balloon gastrostomy tools, disposable overtubes, coaxial and standard needles, papillotomes, electric biopsy forceps, balloon replacement gastrostomy tubes, and endoscopic retrieval devices. The portfolio also includes percutaneous endoscopic gastroscopy tools, color video cameras, and the AquaShield System for CO₂ management in endoscopic procedures.
The company’s devices are classified under Class II in the U.S. and are listed via FDA 510(k) clearance. The portfolio is regulated under U.S. medical device laws, and the manufacturer is based in the United States.
Catalogue
Search and filter all 96 devicesShowing 1-50 of 96
Company details
- EUDAMED SRN
- US-MF-000017968
- FDA FEI number
- 1000122656
- EU VAT number
- 34-148202400
- EUDAMED status
- Active
- EUDAMED registered name
- United States Endoscopy Group, Inc.
- EUDAMED abbreviated name
- Also trading as US Endoscopy
- Registered address
- 5976, Heisley Rd, 44060, Mentor, Ohio, United States
- Website
- www.steris.com
- facebook.com/steriscorporate
- [email protected]
- Phone
- +353 (57) 860 6877
- PRRC contact
- Becky Aldhizer
From the company website
STERIS is a leading global provider of products and services that support patient care with an emphasis on infection prevention.
Frequently asked questions
How many devices does United States Endoscopy Group, Inc. have in the registry?
The registry currently lists 96 devices for United States Endoscopy Group, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list United States Endoscopy Group, Inc.'s devices?
Among its 50 most recently registered devices, United States Endoscopy Group, Inc. has devices listed in FDA 510(k) (50 devices).
What risk classes do United States Endoscopy Group, Inc.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for United States Endoscopy Group, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from United States Endoscopy Group, Inc. in the registry?
The most recently registered devices listed for United States Endoscopy Group, Inc. include U.S. ENDOSCOPY PULL PEG KIT & U.S. ENDOSCOPY GUIDEWIRE PEG KIT, CONCENTRIC BALLOON GOOGLE, DISPOSABLE OVERTUBE and COAXIAL NEEDLE.