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Skil-Care Corp.

United StatesFDA applicant, unverified FDA FEI 3000214954

Devices
20
Registrations
FDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA FEI

Catalogue20

Newest first, rows 1-20 of 20

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Rows 1-20 of 20

Company details

FDA FEI number
3000214954
Address
20 Jones Street, STE 2, New Rochelle, NY, 10801

Frequently asked questions

How many devices does Skil-Care Corp. have in the registry?

The registry currently lists 20 devices for Skil-Care Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Skil-Care Corp.'s devices?

Among its 20 most recently registered devices, Skil-Care Corp. has devices listed in FDA 510(k) (20 devices).

What risk classes do Skil-Care Corp.'s devices fall under?

Among its 20 most recently registered devices, the classes recorded for Skil-Care Corp.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Skil-Care Corp. in the registry?

The most recently registered devices listed for Skil-Care Corp. include LIMB HOLDERS-REUSABLE/LIMB HOLDERS-DISPOSABLE/QUICK-CUFF LIMB HOLDER, DOUBLE SUPPORT PONCHO/SLIDER PONCHO, SAFETY PONCHO/SHOULDER STRAP PONCHO and EZ ON SAFETY PONCHO.

Generated automatically from registry data and not verified by a human reviewer.