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Sign in to claim this brandAmerisourcebergen 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
- —
- Website
- elastictherapy.com
- —
- —
- [email protected]
- Phone
- 336-625-0529
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 007914906
Catalogue (86)
Page 2 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Good Neighbor Pharmacy | One Step Ovulation Predictor | FDA UDI | Class I | Active |
| Gnp | 71008GNP | FDA UDI | Class II | Active |
| Good Neighbor | 6116108 | FDA UDI | Class I | Active |
| Good Neighbor Pharmarcy | 40-19015-144 | FDA UDI | Class I | Active |
| Good Neighbor Pharmacy | 611646 | FDA UDI | Class II | Active |
| Gnp | 09562GNP | FDA UDI | Class II | Active |
| Gnp | 09583GNP | FDA UDI | Class II | Active |
| Gnp | 09583GNP | FDA UDI | Class II | Active |
| Good Neighbor | 6116103 | FDA UDI | Class I | Active |
| Good Neighbor Pharmacy | KD-118 | FDA UDI | Class II | Active |
| Good Neighbor Pharmacy | 611646 | FDA UDI | Class II | Active |
| Gnp | 71009GNP | FDA UDI | Class II | Active |
| Good Neighbor Pharmacy | KD-235 | FDA UDI | Class II | Active |
| Good Neighbor | 10217181 | FDA UDI | Class II | Active |
| Good Neighbor Pharmacy One Step Pregnancy Test | FPPL | FDA UDI | Class II | Unknown |
| Good Neighbor | 10277686 | FDA UDI | Class II | Active |
| Good Neighbor | 90-510 | FDA UDI | Class II | Active |
| Good Neighbor | 6116108 | FDA UDI | Class I | Active |
| Good Neighbor Pharmacy | 700 | FDA UDI | Class II | Active |
| Good Neighbor | 90-363 | FDA UDI | Class II | Active |
| Good Neighbor | 6116101 | FDA UDI | Class I | Active |
| Good Neighbor Pharmacy | F406-906GP | FDA UDI | U | Active |
| Good Neighbor | 90-553 | FDA UDI | Class II | Active |
| Good Neighbor | 90-5501 | FDA UDI | Class II | Active |
| Good Neighbor | 611664 | FDA UDI | Class I | Active |
| Good Neighbor Pharmacy | 10249687 | FDA UDI | Class II | Active |
| Good Neighbor Pharmacy | KI-8170 | FDA UDI | Class II | Active |
| Good Neighbor | 6116101 | FDA UDI | Class I | Active |
| Good Neighbor | Advanced Early Result Pregnancy Test | FDA UDI | Class II | Unknown |
| Good Neighbor Pharmacy | BP3AR1-4DABC | FDA UDI | Class II | Active |
| Good Neighbor Pharmacy One Step Pregnancy Test | FPPL | FDA UDI | Class II | Unknown |
| Good Neighbor | 90-348 | FDA UDI | Class II | Active |
| Good Neighbor | 6194 | FDA UDI | Class I | Active |
| Good Neighbor Pharmacy | One Step Pregnancy Test | FDA UDI | Class II | Unknown |
| Good Neighbor Pharmacy | 611646 | FDA UDI | Class II | Active |
| Good Neighbor Pharmacy | 10231717 | FDA UDI | Class II | Active |
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