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Hollister, Inc.

United StatesFDA 510(k) applicant, unverified FDA FEI 3003172243

Devices
85
Registrations
FDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA FEI

Catalogue85

Newest first, rows 1-50 of 85

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Rows 1-50 of 85

Showing 1-50 of 85

Company details

FDA FEI number
3003172243
Address
12011 VOLUNTEER BLVD, Mount Juliet, TN, 37122

Frequently asked questions

How many devices does Hollister, Inc. have in the registry?

The registry currently lists 85 devices for Hollister, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Hollister, Inc.'s devices?

Among its 50 most recently registered devices, Hollister, Inc. has devices listed in FDA 510(k) (50 devices).

What risk classes do Hollister, Inc.'s devices fall under?

Among its 50 most recently registered devices, the classes recorded for Hollister, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Hollister, Inc. in the registry?

The most recently registered devices listed for Hollister, Inc. include INCARE INTERMITTENT CATHETER, HEELBO QUILTED TORSO RESTRAINT, INCARE PRESSURE BIOFEEDBACK VAGINAL PRESSURE PROBE AND ANAL PRESSURE PROBE and INCARE PINSITE DRESSING.

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