Ansell Pacific, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Ansell Pacific, Inc. makes
Ansell Pacific, Inc. manufactures latex patient examination gloves and anatomical examination gloves designed for clinical use, including medical and dental procedures. These products are intended to provide barrier protection for healthcare providers during patient examinations and treatments.
The company’s portfolio is classified under FDA’s Class I medical devices and is listed via the 510(k) pathway. These devices are regulated under US jurisdiction, adhering to the requirements of the FDA’s regulatory framework.
Catalogue
Patient Examination Gloves (Latex) Ref K892570
Regimes: 510(k) Registry: 510(k)Anatomical Examination Gloves Ref K892579
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ansell Pacific, Inc. have in the registry?
The registry currently lists 2 devices for Ansell Pacific, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ansell Pacific, Inc.'s devices?
Among its 2 most recently registered devices, Ansell Pacific, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Ansell Pacific, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Ansell Pacific, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Ansell Pacific, Inc. in the registry?
The most recently registered devices listed for Ansell Pacific, Inc. include PATIENT EXAMINATION GLOVES (LATEX) and ANATOMICAL EXAMINATION GLOVES.