Neonatal Corp.
United StatesFDA applicant, unverified
- Devices
- 3
What Neonatal Corp. makes
Neonatal Corp. manufactures single-use surgical tools and breastfeeding support devices, including the AXICUT disposable scalpel for neonatal procedures and the AXICARE breast pump with its accompanying breast shell.
Their products are regulated under FDA 510(k) clearance, with devices classified as Class I and Class II. The company is based in the United States.
Catalogue
Axicut Disposable Scalpel Ref K811707
Regimes: 510(k) Registry: 510(k)Axicare Breast Pump Model Ref K811403
Regimes: 510(k) Registry: 510(k)Axicare Breast Shell Ref K811364
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Neonatal Corp. have in the registry?
The registry currently lists 3 devices for Neonatal Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neonatal Corp.'s devices?
Among its 3 most recently registered devices, Neonatal Corp. has devices listed in FDA 510(k) (3 devices).
What risk classes do Neonatal Corp.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Neonatal Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Neonatal Corp. in the registry?
The most recently registered devices listed for Neonatal Corp. include AXICUT DISPOSABLE SCALPEL, AXICARE BREAST PUMP MODEL and AXICARE BREAST SHELL.