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Sign in to claim this brandAnton Meyer & Co. AG
US
Last updated May 24, 2026
What Anton Meyer & Co. AG makes
Anton Meyer & Co. AG manufactures reusable ophthalmic knives, designed for surgical procedures in eye care. These instruments are intended for precision cutting and dissection during ophthalmic surgeries, ensuring sterile and repeat-use applications in clinical settings.
The company’s products are classified as Class I medical devices under regulatory frameworks, with devices listed in the FDA’s Unique Device Identification (UDI) system. Anton Meyer & Co. AG is based in 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 Anton Meyer & Co. AG manufacture?
Anton Meyer & Co. AG specializes in reusable ophthalmic knives. These instruments are specifically designed for precision cutting and dissection during eye surgeries, ensuring sterile and repeat-use applications in clinical settings. The company’s focus is on ophthalmic tools, particularly those used in surgical procedures.
Where is Anton Meyer & Co. AG based?
Anton Meyer & Co. AG is headquartered in the United States. The company’s location is relevant for understanding its regulatory environment and operational reach, particularly in markets where U.S.-based manufacturers are recognized.
Which regulatory registries list Anton Meyer & Co. AG’s devices?
Anton Meyer & Co. AG’s devices are listed in the FDA’s Unique Device Identification (UDI) system. This registry ensures traceability and transparency in the medical device supply chain, allowing healthcare providers and regulators to identify and verify the devices in use.
How are Anton Meyer & Co. AG’s devices classified under medical device regulations?
Anton Meyer & Co. AG’s ophthalmic knives are classified as Class I medical devices. This classification is typically assigned to devices posing the lowest risk to patients, often involving minimal or non-invasive procedures. Class I devices generally undergo less stringent regulatory scrutiny compared to higher-risk categories.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- meyco.ch
- —
- —
- [email protected]
- Phone
- +41323329111
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 480329390
Catalogue (79)
Page 2 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Amidia | A-NANO-C1306A | FDA UDI | Class I | Active |
| Meyco | ME613-C | FDA UDI | Class I | Active |
| Meyco | ME205 | FDA UDI | Class I | Active |
| Amidia | A-NANO-C1132A | FDA UDI | Class I | Active |
| Meyco | ME133 | FDA UDI | Class I | Active |
| Amidia | A-NANO-SC1123A | FDA UDI | Class I | Active |
| Amidia | A-NANO-SC1100A | FDA UDI | Class I | Active |
| Meyco | ME106 | FDA UDI | Class I | Active |
| Meyco | ME613 | FDA UDI | Class I | Active |
| Meyco | ME100-C | FDA UDI | Class I | Active |
| Amidia | A-NANO-C1130A | FDA UDI | Class I | Active |
| Amidia | A-NANO-C1132-01A | FDA UDI | Class I | Active |
| Meyco | ME202 | FDA UDI | Class I | Active |
| Meyco | ME610-C | FDA UDI | Class I | Active |
| Meyco | ME105 | FDA UDI | Class I | Active |
| Meyco | ME600 | FDA UDI | Class I | Active |
| Amidia | A-NANO-SC1133A | FDA UDI | Class I | Active |
| Meyco | ME203-C | FDA UDI | Class I | Active |
| Amidia | A-NANO-SC1132A | FDA UDI | Class I | Active |
| Meyco | ME450 | FDA UDI | Class I | Active |
| Meyco | ME615 | FDA UDI | Class I | Active |
| Meyco | ME297 | FDA UDI | Class I | Active |
| Meyco | ME435 | FDA UDI | Class I | Active |
| Meyco | ME707 | FDA UDI | Class I | Active |
| Amidia | A-NANO-C1100A | FDA UDI | Class I | Active |
| Amidia | A-NANO-SC1135A | FDA UDI | Class I | Active |
| Meyco | ME630-C | FDA UDI | Class I | Active |
| Amidia | A-NANO-SC1000A | FDA UDI | Class I | Active |
| Amidia | A-NANO-SC1127A | FDA UDI | Class I | Active |
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