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Packroom LLC

United Statesfrom the FDA registration address FDA FEI 3008513424

Packroom LLC is a medical device manufacturer, with 428 devices listed in FDA GUDID as of 12 Nov 2026.

Devices
428
Registrations
FDA
FDA recalls
0

Registry facts

Counted by deviCERTS from registry records, 12 Nov 2026

Registries
  • FDA GUDID 428
Identifiers
  • FDA FEI 3008513424
  • DUNS 015179820

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA FEI

Catalogue428

Newest first, rows 1-50 of 428

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Rows 1-50 of 428

Showing 1-50 of 428

Company details

FDA FEI number
3008513424
DUNS number
015179820
Address
1281 Highway 155 South, Mc Donough, GA, 30253

Frequently asked questions

How many devices does PACKROOM LLC have in the registry?

The registry currently lists 428 devices for PACKROOM LLC. Devices recorded under merged duplicate company entries are counted once.

Which registries list PACKROOM LLC's devices?

Among its 50 most recently registered devices, PACKROOM LLC has devices listed in FDA GUDID (50 devices).

What are the newest devices from PACKROOM LLC in the registry?

The most recently registered devices listed for PACKROOM LLC include NEGA Lithotomy RFID Pack NG115RFA, Pack, CABG Kennestone WK221A, Pack, ENT Bradley BH410 and Kit, Ped Intub Gray 3-5kg NGHS KT7700AINA.

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