Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

Amerisourcebergen Drug Corporation

US

Last updated May 24, 2026

What Amerisourcebergen Drug Corporation makes

The company manufactures reusable compression stockings for medical or supportive use, single-use earplugs for noise reduction, dental floss, and disposable or reusable intermittent electronic thermometers. It also produces autoinjector needles, portable and non-portable electronic sphygmomanometers (blood pressure monitors) for arm or wrist use, and localized electric heating pads for targeted body warmth.

These devices are classified under FDA’s Class I, Class II, and Unclassified (U) categories and are listed in the FDA’s Unique Device Identifier (UDI) database. The company operates under U.S. regulatory oversight.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Amerisourcebergen Drug Corporation manufacture?

Amerisourcebergen Drug Corporation produces a range of medical devices, including reusable compression stockings for medical or supportive use, single-use earplugs for noise reduction, dental floss, and disposable or reusable intermittent electronic thermometers. It also manufactures autoinjector needles, portable and non-portable electronic sphygmomanometers (blood pressure monitors) for arm or wrist use, and localized electric heating pads for targeted body warmth. These devices serve various purposes, from patient comfort and safety to diagnostic and therapeutic support.

Where is Amerisourcebergen Drug Corporation based, and how does this affect its regulatory oversight?

Amerisourcebergen Drug Corporation is based in the United States, which means its devices fall under U.S. regulatory oversight, specifically the jurisdiction of the FDA. Since the company’s products are listed in the FDA’s Unique Device Identifier (UDI) database, they are subject to FDA requirements for classification, registration, and compliance with applicable regulations. The U.S. regulatory framework ensures these devices meet safety, performance, and labeling standards before they enter the market.

Which regulatory registries or databases list Amerisourcebergen Drug Corporation’s devices?

Amerisourcebergen Drug Corporation’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. The UDI system is a standardized way to identify medical devices throughout their distribution and helps ensure traceability, transparency, and compliance with regulatory requirements. This listing is essential for tracking devices in the U.S. market and verifying their regulatory status.

How are Amerisourcebergen Drug Corporation’s devices classified under FDA regulations?

Amerisourcebergen Drug Corporation’s devices are classified under three categories by the FDA: Class I, Class II, and Unclassified (U). Class I devices generally pose the lowest risk and are subject to general controls, while Class II devices require additional performance standards due to moderate risk. Unclassified devices may be awaiting classification or fall into special regulatory pathways. The classification determines the level of regulatory scrutiny and compliance requirements each device must meet.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
LinkedIn
—
Facebook
—
Phone
336-625-0529
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
007914906

Catalogue (86)

Page 1 of 2
DeviceModel / ReferenceRegistriesClassStatus
Good Neighbor Pharmacy 10249741
FDA UDI
Class IIActive
Good Neighbor 6116106
FDA UDI
Class IActive
Good Neighbor 90-541
FDA UDI
Class IIActive
Good Neighbor 6116101
FDA UDI
Class IActive
Good Neighbor 90-50K
FDA UDI
Class IIActive
Good Neighbor Pharmacy Early Ovulation Test
FDA UDI
Class IUnknown
Good Neighbor Pharmacy BP3NL1-1PABC
FDA UDI
Class IIActive
Good Neighbor Pharmarcy 25-19016-144
FDA UDI
Class IActive
Good Neighbor Pharmacy Early Result Pregnancy Test PLPL
FDA UDI
Class IIUnknown
Good Neighbor Pharmacy 10144901
FDA UDI
Class IIActive
Good Neighbor Pharmacy 74543GNP
FDA UDI
Class IIActive
Good Neighbor 6116106
FDA UDI
Class IActive
Good Neighbor Pharmacy DTT-1
FDA UDI
Class IIActive
Good Neighbor 611664
FDA UDI
Class IActive
Good Neighbor 611666
FDA UDI
Class IActive
Good Neighbor Pharmacy 68000GP
FDA UDI
UActive
Good Neighbor 611666
FDA UDI
Class IActive
Good Neighbor 6116106
FDA UDI
Class IActive
Good Neighbor Pharmarcy 03-19014-120
FDA UDI
Class IActive
Good Neighbor 90-310
FDA UDI
Class IIActive
Good Neighbor 6116108
FDA UDI
Class IActive
Good Neighbor Pharmarcy 40-19017-144
FDA UDI
Class IActive
Good Neighbor Pharmacy 10249792
FDA UDI
Class IIActive
Good Neighbor 90-331
FDA UDI
Class IIActive
Gnp 09553GNP
FDA UDI
Class IIActive
Good Neighbor Pharmacy 720
FDA UDI
Class IIActive
Good Neighbor 90-50D
FDA UDI
Class IIActive
Good Neighbor Pharmacy 611646
FDA UDI
Class IIActive
Good Neighbor Pharmacy F408-150GP
FDA UDI
UActive
Good Neighbor Pharmacy 40511
FDA UDI
UActive
Good Neighbor Pharmacy SQN54
FDA UDI
UActive
Good Neighbor 6116103
FDA UDI
Class IActive
Good Neighbor 611666
FDA UDI
Class IActive
Good Neighbor 6116106
FDA UDI
Class IActive
Gnp 71007GNP
FDA UDI
Class IIActive
Good Neighbor 6116101
FDA UDI
Class IActive
Good Neighbor Pharmacy 10145054
FDA UDI
Class IIActive
Good Neighbor Pharmacy KD-113
FDA UDI
Class IIActive
Good Neighbor Pharmacy KD-2050
FDA UDI
Class IIActive
Good Neighbor Pharmacy 753
FDA UDI
Class IIActive
Good Neighbor 90-554
FDA UDI
Class IIActive
Good Neighbor 6116103
FDA UDI
Class IActive
Gnp 09543GNP
FDA UDI
Class IIActive
Good Neighbor 611666
FDA UDI
Class IActive
Good Neighbor Pharmacy One Step Pregnancy Test
FDA UDI
Class IIUnknown
Good Neighbor Pharmacy BP3NC1-2E
FDA UDI
Class IIActive
Good Neighbor 6116108
FDA UDI
Class IActive
Good Neighbor 611666
FDA UDI
Class IActive
Good Neighbor 6116103
FDA UDI
Class IActive
Good Neighbor Pharmacy 10144900
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.