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Sign in to claim this brandPROGRESSIVE MEDICAL INSTRUMENTATION INC
US
Last updated May 27, 2026
What PROGRESSIVE MEDICAL INSTRUMENTATION INC makes
Progressive Medical Instrumentation Inc manufactures reusable surgical instruments for endoscopic procedures, including rigid tissue manipulation forceps, bipolar electrosurgical handpieces, and optical arthroscopes. Their portfolio also includes orthopaedic tools like joint/limb rongeurs, coronary artery clamps, and reusable laryngoscopes for intubation. Additional products feature reusable irrigation/aspiration handpieces and electrical connection cables for medical devices.
The company’s devices are classified under FDA regulations as Class I and Class II, with most listed in the FDA’s Unique Device Identifier (UDI) database. These instruments are intended for use in the United States, adhering to applicable medical device standards and registration requirements.
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 Progressive Medical Instrumentation Inc manufacture?
Progressive Medical Instrumentation Inc specializes in reusable surgical instruments primarily used in endoscopic and orthopaedic procedures. Their portfolio includes rigid endoscopic tissue manipulation forceps, bipolar electrosurgical handpieces, optical arthroscopes, coronary artery clamps, laryngoscopes for intubation, orthopaedic rongeurs, irrigation/aspiration handpieces, and reusable electrical connection cables. These devices are designed for repeated use in clinical settings, adhering to standards for reusable medical instruments.
Where is Progressive Medical Instrumentation Inc based, and what does that mean for its devices?
Progressive Medical Instrumentation Inc is based in the United States. This means their devices are developed and manufactured in compliance with U.S. medical device regulations, including registration requirements, quality standards, and classification rules. Their products are intended for use within the U.S. market and must meet FDA-specific criteria for safety, performance, and labeling.
Which regulatory registries or databases list devices from Progressive Medical Instrumentation Inc?
Devices from Progressive Medical Instrumentation Inc are listed in the FDA’s Unique Device Identifier (UDI) database. The UDI system ensures traceability and transparency in the medical device supply chain, allowing healthcare providers, regulators, and other stakeholders to identify and verify specific devices through standardized identifiers. This listing helps streamline regulatory oversight and device tracking.
How are devices from Progressive Medical Instrumentation Inc classified under FDA regulations?
Devices from Progressive Medical Instrumentation Inc are classified under the FDA’s medical device classification system as either Class I or Class II. Class I devices generally pose the lowest risk and may require general controls, while Class II devices involve a higher risk and require special controls to ensure safety and effectiveness. The classification depends on factors like the device’s intended use, potential risks, and the body area it interacts with, as outlined in the FDA’s regulatory framework.
Why do some devices from Progressive Medical Instrumentation Inc appear multiple times in the example list?
The repeated examples of devices like AVALIGN and ELMED in the list reflect the company’s portfolio of reusable surgical instruments, where certain models may serve multiple purposes or variations within the same category. For instance, a single device model (e.g., ELMED) could be used across different endoscopic procedures or in various surgical contexts, depending on its design and intended use. This repetition highlights the versatility of their reusable instruments rather than indicating distinct, separate devices.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- pmirepairs.com
- —
- —
- [email protected]
- Phone
- 5022671100
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 131054074
Catalogue (46)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Avalign | PMI-LK75-2974/45 | FDA UDI | Class II | Active |
| Elmed | PMI52-25506B1 | FDA UDI | Class II | Active |
| Elmed | PMI52-25560A1 | FDA UDI | Class II | Active |
| Avalign | PMI-RD-D | FDA UDI | Class II | Active |
| Elmed | PMI52-25547A1 | FDA UDI | Class II | Active |
| Elmed | PMI5023 | FDA UDI | Class II | Active |
| Elmed | PMI-PMI5210581 | FDA UDI | Class II | Active |
| Elmed | PMI52-25540B10 | FDA UDI | Class II | Active |
| Avalign | PMI-HD-D | FDA UDI | Class II | Active |
| Elmed | PMI37-500707 | FDA UDI | Class II | Active |
| Elmed | PMI403658 | FDA UDI | Class I | Active |
| Elmed | PMI-PMI5210582 | FDA UDI | Class II | Active |
| Elmed | PMI52-25560B1 | FDA UDI | Class II | Active |
| Avalign | PMI-LK75-2974/09 | FDA UDI | Class II | Active |
| Elmed | PMI52-50515 | FDA UDI | Class II | Active |
| Elmed | PMI52-51015 | FDA UDI | Class II | Active |
| Elmed | PMI52-20510010 | FDA UDI | Class II | Active |
| Elmed | PMI52-00546 | FDA UDI | Class II | Active |
| Avalign | PMI-B3-VB | FDA UDI | Class II | Active |
| Avalign | PMI-B-3V | FDA UDI | Class II | Active |
| Avalign | PMI-ABB-22V | FDA UDI | Class II | Active |
| Elmed | PMI59-8010BM | FDA UDI | Class II | Active |
| Avalign | PMI-HD-S | FDA UDI | Class II | Active |
| Elmed | PMI425301 | FDA UDI | Class I | Active |
| Elmed | PMI422010 | FDA UDI | Class I | Active |
| Elmed | PMI37-500912W | FDA UDI | Class II | Active |
| Avalign | PMI-DC-1-B | FDA UDI | Class II | Active |
| Avalign | PMI-ABB-11V | FDA UDI | Class II | Active |
| Avalign | PMI-8361-00 | FDA UDI | Class II | Active |
| Elmed | PMI-PMI5220583 | FDA UDI | Class II | Active |
| Elmed | PMI23-40045STR | FDA UDI | Class I | Active |
| Elmed | PMI52-25510B1 | FDA UDI | Class II | Active |
| Elmed | PMI52-205100 | FDA UDI | Class II | Active |
| Avalign | PMI-B-2V | FDA UDI | Class II | Active |
| Elmed | PMI-PMI5220582 | FDA UDI | Class II | Active |
| Elmed | PMI37-500912B | FDA UDI | Class II | Active |
| Elmed | PMI52-105101 | FDA UDI | Class II | Active |
| Elmed | PMI4207021 | FDA UDI | Class I | Active |
| Elmed | PMI52-25571A1 | FDA UDI | Class II | Active |
| Elmed | PMI52-25541A12 | FDA UDI | Class II | Active |
| Elmed | PMI52-00548 | FDA UDI | Class II | Active |
| Avalign | PMI-ABB-33V | FDA UDI | Class II | Active |
| Elmed | PMI52-25566B1 | FDA UDI | Class II | Active |
| Elmed | PMI52-00532 | FDA UDI | Class II | Active |
| Elmed | PMI52-52582 | FDA UDI | Class II | Active |
| Elmed | PMI59-5009 | FDA UDI | Class II | Active |
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