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Sign in to claim this brandM.S.T. MEDICAL SURGERY TECHNOLOGIES LTD
US
Last updated May 24, 2026
What M.S.T. MEDICAL SURGERY TECHNOLOGIES LTD makes
M.S.T. Medical Surgery Technologies Ltd produces laparoscopic accessories and assist systems, including molded clipper packages, sterile component kits, and single-procedure kits for 5mm and 10mm instruments. Their portfolio also includes the AutoLap system, which features a touchscreen-controlled assist arm unit, curved bars, and sterile drapes designed for minimally invasive surgical procedures. These devices are engineered to support precise handling of surgical instruments during laparoscopic surgery.
The company’s devices are classified as Class II under FDA regulations and are listed in the FDA’s 510(k) and Unique Device Identifier (UDI) databases. The manufacturer operates from the United States, adhering to regulatory requirements for surgical assist systems and laparoscopic accessories.
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 M.S.T. Medical Surgery Technologies Ltd manufacture?
M.S.T. Medical Surgery Technologies Ltd specializes in laparoscopic accessories and assist systems. Their product range includes molded clipper packages (such as the 5mm and 10mm versions), sterile component kits, single-procedure kits, and the AutoLap system. This system comprises a touchscreen-controlled assist arm unit, sterile drapes, and accessories like curved bars and bars, all designed to aid in minimally invasive surgical procedures.
Where is M.S.T. Medical Surgery Technologies Ltd based?
M.S.T. Medical Surgery Technologies Ltd is headquartered in the United States. The company’s location ensures compliance with U.S. regulatory standards for surgical assist systems and laparoscopic accessories, which are critical for devices used in minimally invasive procedures.
Which regulatory registries list M.S.T. Medical Surgery Technologies Ltd’s devices?
M.S.T. Medical Surgery Technologies Ltd’s devices are listed in the FDA’s 510(k) premarket notification database and the Unique Device Identifier (UDI) system. These registries help track and verify the authorization status of Class II devices, ensuring transparency and compliance with U.S. medical device regulations.
How are M.S.T. Medical Surgery Technologies Ltd’s devices classified under FDA regulations?
M.S.T. Medical Surgery Technologies Ltd’s devices fall under Class II classification by the FDA. This classification applies to devices that pose moderate risk and require special controls—such as performance standards or post-market surveillance—to ensure safety and effectiveness. The company’s products, including the AutoLap system and laparoscopic accessories, meet these regulatory requirements.
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
- 649827193
Catalogue (29)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Molded Laparoscopic Clipper Package- 5mm | ASS06015US | FDA UDI | Class II | Active |
| AutoLap Sterile Components Kit Package- Clip, 10mm | ASS02430US | FDA UDI | Class II | Active |
| AutoLap Single Procedure Kit Pack (Ring, 10mm) | ASS06510US | FDA UDI | Class II | Active |
| AutoLap | SYS00002 | FDA UDI | Class II | Active |
| AutoLap Sterile Drape | ASS07022US | FDA UDI | Class II | Active |
| AutoLap Curved ARM | MST-03-0101 | FDA UDI | Class II | Unknown |
| AutoLap Touch Screen | ASS06010 | FDA UDI | Class II | Active |
| AutoLap ARM | MST-02-0101 | FDA UDI | Class II | Unknown |
| AutoLap Cart | MST-10-0100 | FDA UDI | Class II | Unknown |
| AutoLap ARM Unit | MST-15-0100 | FDA UDI | Class II | Active |
| AutoLap Single Procedure Kit Pack- (Ring, 5mm) | ASS06520US | FDA UDI | Class II | Active |
| AutoLap Curved Bar | MST-03-0104 | FDA UDI | Class II | Active |
| Clip Command Unit Package | ASS03002 | FDA UDI | Class II | Active |
| AutoLap Sterile Components Kit Package- Ring, 5mm | ASS02140US | FDA UDI | Class II | Active |
| AutoLap Bar | MST-03-0102 | FDA UDI | Class II | Active |
| AutoLap Sterile Components Kit Package- Ring, 10mm | ASS02130US | FDA UDI | Class II | Active |
| Ring Command Unit Package | ASS05002 | FDA UDI | Class II | Active |
| AutoLap Sterile Drape | ASS07018US | FDA UDI | Class II | Unknown |
| AutoLap Single Procedure Kit Pack (Clip, 10mm) | ASS06610US | FDA UDI | Class II | Active |
| AutoLap PU | ASS06008US | FDA UDI | Class II | Active |
| Autolap Cart | MST-12-0100 | FDA UDI | Class II | Active |
| AutoLap Single procedure kit Pack (Clip, 5mm) | ASS06620US | FDA UDI | Class II | Active |
| AutoLap Bar Extender | MST-02-0111 | FDA UDI | Class II | Active |
| AutoLap Streile Components Kit Package- Clip, 5mm | ASS02440US | FDA UDI | Class II | Active |
| AutoLap Positioner | MST-13-0114 | FDA UDI | Class II | Active |
| AutoLap ARM Unit Package | ASS06030 | FDA UDI | Class II | Active |
| Molded Laparoscopic Clippers package- 10mm | ASS06014US | FDA UDI | Class II | Active |
| Autolap System | K131375 | FDA 510(k) | Class II | Active |
| Autolap System | K152848 | FDA 510(k) | Class II | Active |
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