Lovell-Schenck, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Lovell-Schenck, Inc. makes
Lovell-Schenck, Inc. manufactures non-sterile clinical-style glove liners and surgeon’s glove accessories, designed to enhance procedural comfort and fit during medical procedures.
These products are classified as Class I devices under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Non-Sterile Clinical Style Paraderm Glove Liner Ref K910890
Regimes: 510(k) Registry: 510(k)Paraderm(Tm) Surgeon's Glove Accessory Ref K904903
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lovell-Schenck, Inc. have in the registry?
The registry currently lists 2 devices for Lovell-Schenck, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lovell-Schenck, Inc.'s devices?
Among its 2 most recently registered devices, Lovell-Schenck, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Lovell-Schenck, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Lovell-Schenck, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Lovell-Schenck, Inc. in the registry?
The most recently registered devices listed for Lovell-Schenck, Inc. include NON-STERILE CLINICAL STYLE PARADERM GLOVE LINER and PARADERM(TM) SURGEON'S GLOVE ACCESSORY.