Kindly Assoc., Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Kindly Assoc., Inc. makes
Kindly Assoc., Inc. manufactures latex patient examination gloves, designed for single-use in clinical and medical settings to maintain hygiene and reduce infection risk during examinations.
These products are classified as Class I devices under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
Patient Examination Gloves (Latex) Ref K891822
Regimes: 510(k) Registry: 510(k)Patient Examination Gloves (Latex) Ref K892037
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kindly Assoc., Inc. have in the registry?
The registry currently lists 2 devices for Kindly Assoc., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kindly Assoc., Inc.'s devices?
Among its 2 most recently registered devices, Kindly Assoc., Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Kindly Assoc., Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Kindly Assoc., Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Kindly Assoc., Inc. in the registry?
The most recently registered devices listed for Kindly Assoc., Inc. include PATIENT EXAMINATION GLOVES (LATEX).