Raewiks, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Raewiks, Inc. makes
Raewiks, Inc. manufactures latex patient examination gloves designed for clinical use, providing a barrier for medical professionals during examinations and procedures.
These devices are classified as Class I under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Patient Examination Gloves (Latex) Ref K891256
Regimes: 510(k) Registry: 510(k)Patient Examination Gloves (Latex) Ref K892167
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Raewiks, Inc. have in the registry?
The registry currently lists 2 devices for Raewiks, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Raewiks, Inc.'s devices?
Among its 2 most recently registered devices, Raewiks, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Raewiks, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Raewiks, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Raewiks, Inc. in the registry?
The most recently registered devices listed for Raewiks, Inc. include PATIENT EXAMINATION GLOVES (LATEX).