Intermarket Latex, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Intermarket Latex, Inc. makes
Intermarket Latex, Inc. manufactures sterile disposable surgical gloves designed for single-use in medical and surgical procedures. These gloves are intended to provide a barrier against contamination during clinical interventions.
The company’s products fall under FDA Class I devices and are listed via the 510(k) pathway. The manufacturer operates from the United States.
Catalogue
Sterile Disposable Surgical Gloves Ref K830635
Regimes: 510(k) Registry: 510(k)Sterile Disposable Surgical Gloves Ref K812421
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Intermarket Latex, Inc. have in the registry?
The registry currently lists 2 devices for Intermarket Latex, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Intermarket Latex, Inc.'s devices?
Among its 2 most recently registered devices, Intermarket Latex, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Intermarket Latex, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Intermarket Latex, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Intermarket Latex, Inc. in the registry?
The most recently registered devices listed for Intermarket Latex, Inc. include STERILE DISPOSABLE SURGICAL GLOVES.