Aor-Sullivan
Country not established
- Devices
- 2
What Aor-Sullivan makes
Aor-Sullivan manufactures protective overgloves designed to provide barrier protection for healthcare workers and patients. These products are intended for single-use applications in clinical settings to reduce exposure to bodily fluids and contaminants during medical procedures.
The company’s portfolio is classified under FDA’s Class I regulatory category, with devices listed via the 510(k) pathway. These products are registered in the United States, adhering to FDA compliance requirements for low-risk medical devices.
Catalogue
Modified Aor-Sullivan Protective Overglove Ref K902016
Regimes: 510(k) Registry: 510(k)Aor-Sullivan Protective Overglove Ref K893118
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Aor-Sullivan have in the registry?
The registry currently lists 2 devices for Aor-Sullivan. Devices recorded under merged duplicate company entries are counted once.
Which registries list Aor-Sullivan's devices?
Among its 2 most recently registered devices, Aor-Sullivan has devices listed in FDA 510(k) (2 devices).
What risk classes do Aor-Sullivan's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Aor-Sullivan's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Aor-Sullivan in the registry?
The most recently registered devices listed for Aor-Sullivan include MODIFIED AOR-SULLIVAN PROTECTIVE OVERGLOVE and AOR-SULLIVAN PROTECTIVE OVERGLOVE.