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Sign in to claim this brandCLINT PHARMACEUTICALS, INC.
US
Last updated May 25, 2026
What CLINT PHARMACEUTICALS, INC. makes
Clint Pharmaceuticals, Inc. manufactures single-use spinal needles and non-threaded epidural needles designed for medical procedures. These devices are intended for one-time use in spinal and epidural injections, ensuring precision and sterility in clinical settings.
The company’s products fall under FDA Class II medical devices and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates within the regulatory framework of the United States.
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 Clint Pharmaceuticals, Inc. manufacture?
Clint Pharmaceuticals, Inc. specializes in single-use medical devices for spinal and epidural procedures. Their primary products include spinal needles and non-threaded epidural needles, designed for precision and sterility in clinical settings. These devices are intended for one-time use during injections, ensuring safety and reliability in medical applications.
Where is Clint Pharmaceuticals, Inc. based, and how does this affect its regulatory compliance?
Clint Pharmaceuticals, Inc. is based in the United States. As a U.S.-based manufacturer, its devices must comply with FDA regulations, including classification under the FDA’s medical device hierarchy. The company’s products fall under FDA Class II, which typically requires additional controls beyond general good manufacturing practices to ensure safety and effectiveness.
Which regulatory registries or databases list Clint Pharmaceuticals, Inc.’s devices?
Clint Pharmaceuticals, Inc.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency in the medical device supply chain, allowing healthcare providers, regulators, and other stakeholders to verify product details and compliance with U.S. regulatory requirements.
How are Clint Pharmaceuticals, Inc.’s devices classified by regulatory authorities?
Clint Pharmaceuticals, Inc.’s devices are classified as FDA Class II medical devices. This classification indicates that while they pose moderate risks, they require special controls beyond general controls to ensure their safety and performance. Class II devices often involve performance standards, post-market surveillance, or labeling requirements to mitigate potential risks.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 609197785
Catalogue (35)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| AccuTip | AT2580Q | FDA UDI | Class II | Active |
| AccuTip | AT2035TDS | FDA UDI | Class II | Active |
| AccuTip | AT2045T | FDA UDI | Class II | Active |
| AccuTip | AT1835C | FDA UDI | Class II | Active |
| AccuTip | AT18G60T | FDA UDI | Class II | Active |
| AccuTip | AT2035Q | FDA UDI | Class II | Active |
| AccuTip | AT2535Q | FDA UDI | Class II | Active |
| AccuTip | AT2250QS | FDA UDI | Class II | Active |
| AccuTip | AT2060T | FDA UDI | Class II | Active |
| AccuTip | AT2035T | FDA UDI | Class II | Active |
| AccuTip | AT2270Q | FDA UDI | Class II | Active |
| AccuTip | AT1835T | FDA UDI | Class II | Active |
| AccuTip | AT2260C | FDA UDI | Class II | Active |
| AccuTip | AT2525Q | FDA UDI | Class II | Active |
| AccuTip | AT1860C | FDA UDI | Class II | Active |
| AccuTip | AT2225Q | FDA UDI | Class II | Active |
| AccuTip | AT2370Q | FDA UDI | Class II | Active |
| AccuTip | AT1845T | FDA UDI | Class II | Active |
| AccuTip | AT2035C | FDA UDI | Class II | Active |
| AccuTip | AT2260QS | FDA UDI | Class II | Active |
| AccuTip | AT2560Q | FDA UDI | Class II | Active |
| AccuTip | AT1735T | FDA UDI | Class II | Active |
| AccuTip | AT2335Q | FDA UDI | Class II | Active |
| AccuTip | AT2350Q | FDA UDI | Class II | Active |
| AccuTip | AT1860Q | FDA UDI | Class II | Active |
| AccuTip | AT2550Q | FDA UDI | Class II | Active |
| AccuTip | AT1835Q | FDA UDI | Class II | Active |
| AccuTip | AT1825T | FDA UDI | Class II | Active |
| AccuTip | AT2060Q | FDA UDI | Class II | Active |
| AccuTip | AT2360Q | FDA UDI | Class II | Active |
| AccuTip | AT2570Q | FDA UDI | Class II | Active |
| AccuTip | AT2235Q | FDA UDI | Class II | Active |
| AccuTip | AT1760T | FDA UDI | Class II | Active |
| AccuTip | AT2280Q | FDA UDI | Class II | Active |
| AccuTip | AT2230Q | FDA UDI | Class II | Active |
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