Shenzhen Lyttop Healthcare Limited
ChinaFDA applicant, unverified
- Devices
- 2
What Shenzhen Lyttop Healthcare Limited makes
Shenzhen Lyttop Healthcare Limited manufactures single-use, non-antimicrobial surgical and medical face masks designed for healthcare settings. These products are intended for one-time use to protect patients and healthcare workers from airborne contaminants during medical procedures.
The company’s portfolio is regulated under FDA Class II devices and is listed in the FDA’s 510(k) and UDI registries. The manufacturer is based in the United States.
Catalogue
- Registry: GUDID
Medical Face Mask Ref K211353
Regimes: 510(k) Registry: 510(k)
Company details
- DUNS number
- 721969440
Frequently asked questions
How many devices does Shenzhen Lyttop Healthcare Limited have in the registry?
The registry currently lists 2 devices for Shenzhen Lyttop Healthcare Limited. Devices recorded under merged duplicate company entries are counted once.
Which registries list Shenzhen Lyttop Healthcare Limited's devices?
Among its 2 most recently registered devices, Shenzhen Lyttop Healthcare Limited has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Shenzhen Lyttop Healthcare Limited's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Shenzhen Lyttop Healthcare Limited's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Shenzhen Lyttop Healthcare Limited in the registry?
The most recently registered devices listed for Shenzhen Lyttop Healthcare Limited include Lyttop LT0819 and Medical Face Mask.