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Sign in to claim this brandMinimally Invasive Devices, LLC
US
Last updated May 23, 2026
What Minimally Invasive Devices, LLC makes
Minimally Invasive Devices, LLC produces single-use endoscope lens cleaners and gas/fluid solutions, as well as reusable laparoscopic trocar blades. Their portfolio includes antifog solutions designed for endoscopes, marketed under the FloShield brand with variations like FloShield/Air and FloShield/Plus.
These devices are classified as Class II under FDA regulations and are authorised through the 510(k) pathway and listed in the FDA’s Unique Device Identifier (UDI) database. The company operates from 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 Minimally Invasive Devices, LLC manufacture?
Minimally Invasive Devices, LLC specializes in three primary categories: single-use endoscope lens cleaners and gas/fluid solutions, reusable laparoscopic trocar blades, and endoscope antifog solutions. Their most common products fall under the FloShield brand, which includes variations like FloShield/Air and FloShield/Plus, designed to maintain endoscope clarity and functionality during procedures.
Where is Minimally Invasive Devices, LLC based?
The company is headquartered in the United States. This location aligns with its regulatory compliance requirements, particularly for FDA-authorised devices, ensuring adherence to domestic medical device regulations.
Which regulatory registries or databases list Minimally Invasive Devices, LLC’s devices?
Minimally Invasive Devices, LLC’s devices are listed in the FDA’s 510(k) database, which tracks premarket notifications for Class II devices, and the FDA’s Unique Device Identifier (UDI) database. These registries ensure traceability and compliance tracking for authorised medical devices.
How are Minimally Invasive Devices, LLC’s devices classified under FDA regulations?
All devices produced by Minimally Invasive Devices, LLC fall under Class II classification by the FDA. This classification applies to devices that pose moderate risk and require special controls beyond general controls to ensure safety and effectiveness, such as 510(k) premarket notifications.
What is the reasoning behind the FloShield brand’s variations (e.g., FloShield/Air vs. FloShield/Plus)?
The FloShield brand variations likely cater to specific clinical needs: FloShield/Air may be formulated for environments requiring air-based cleaning or drying, while FloShield/Plus could offer enhanced properties like extended antifog duration or additional antimicrobial benefits. These distinctions help healthcare providers select solutions tailored to their endoscope maintenance protocols.
AI-generated from registry data and not verified by a human reviewer.
Information
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- US
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Catalogue (80)
Page 2 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| FloShield 10mm Endoscopic Cannula | FRT-10C | FDA UDI | Class II | Active |
| FloShield/Plus | FSB-02-0500 | FDA UDI | Class II | Active |
| Robotic FloShield/Plus | RTS1 | FDA UDI | Class II | Active |
| FloShield/Air | FSB-04-1030T | FDA UDI | Class II | Active |
| Robotic FloShield/Plus | FSR-05-8500U | FDA UDI | Class II | Active |
| FloShield/Plus | FSS-04-1045 | FDA UDI | Class II | Active |
| FloShield/Plus | FSB-02-0530 | FDA UDI | Class II | Active |
| FloShield/Air | FSS-01-0500T | FDA UDI | Class II | Active |
| FloShield/Air | FSS-01-1000T | FDA UDI | Class II | Active |
| FloShield/Air | FSS-02-0500T | FDA UDI | Class II | Active |
| FloShield/Plus | FSB-02-1045 | FDA UDI | Class II | Active |
| FloShield/Plus | FSS-02-0545 | FDA UDI | Class II | Active |
| FloShield/Plus | FSS-04-1000 | FDA UDI | Class II | Active |
| FloShield/Plus | FSS-01-0545 | FDA UDI | Class II | Active |
| FloShield/Plus | FSB-04-1045 | FDA UDI | Class II | Active |
| FloShield/Air | FSB-02-1030T | FDA UDI | Class II | Active |
| FloShield/Plus | FSS-01-0530 | FDA UDI | Class II | Active |
| FloShield 10mm Full Blunt Obturator | FRT-10B | FDA UDI | Class II | Active |
| FloShield/Plus | FSB-02-1030 | FDA UDI | Class II | Active |
| FloShield/Plus | FSS-02-0500 | FDA UDI | Class II | Active |
| Robotic FloShield/Plus | FSR-05-8500U | FDA UDI | Class II | Active |
| FloShield/Plus | FSB-02-1000 | FDA UDI | Class II | Active |
| FloShield/Plus | FSS-02-1000 | FDA UDI | Class II | Active |
| FloShield/Air | FSS-02-1000T | FDA UDI | Class II | Active |
| FloShield/Air | FSS-02-1030T | FDA UDI | Class II | Active |
| FloShield/Plus | FSB-01-1030 | FDA UDI | Class II | Active |
| Clear-Vu System, Models: Cvl-01-1000, Cvl-01-1030, Cvl-01-1045 | K080613 | FDA 510(k) | Class II | Active |
| Floshield 10mm Endoscopic Cannula And Blunt Obturator, Floshield 10mm Endoscopic Cannula, Floshield 10mm Blunt Obturator | K141272 | FDA 510(k) | Class II | Active |
| FloShield 10mm Endoscopic Cannula and Conical Blunt Obturator, FloShield 10mm Endoscopic Cannula, FloShield 10mm Conical Blunt Obturator | K150705 | FDA 510(k) | Class II | Active |
| Defogging And Cleaning Solution- Flo-X | K102452 | FDA 510(k) | Class II | Active |
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