Medical Engineering Laboratory, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Medical Engineering Laboratory, Inc. makes
Medical Engineering Laboratory, Inc. manufactures flexible gastrointestinal biopsy forceps and tri-talon retrieval forceps, designed for endoscopic procedures to obtain tissue samples and remove foreign objects from the digestive tract.
These devices are classified as Class II under FDA regulations and are listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Gastrointestinal Flexible Biospy Forceps Ref K873248
Regimes: 510(k) Registry: 510(k)Tri Talon Retrieval Forceps Ref K973071
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medical Engineering Laboratory, Inc. have in the registry?
The registry currently lists 2 devices for Medical Engineering Laboratory, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medical Engineering Laboratory, Inc.'s devices?
Among its 2 most recently registered devices, Medical Engineering Laboratory, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Medical Engineering Laboratory, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Medical Engineering Laboratory, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medical Engineering Laboratory, Inc. in the registry?
The most recently registered devices listed for Medical Engineering Laboratory, Inc. include GASTROINTESTINAL FLEXIBLE BIOSPY FORCEPS and TRI TALON RETRIEVAL FORCEPS.