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Sign in to claim this brandMaco International
US
Last updated May 23, 2026
What Maco International makes
Maco International manufactures reusable and single-use laryngoscope blades and handles, including conventional, fiber optic, and LED variants. Their product line also includes reusable airway tube forceps, designed for use in airway management procedures. Examples include Macintosh and Miller blade types, both in disposable and reusable forms, as well as specialized fiber optic and LED-enhanced designs.
The company’s devices are classified as Class I under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. These products are intended for use in the United States, adhering to applicable medical device standards and compliance 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 Maco International manufacture?
Maco International specializes in laryngoscope blades and handles, offering both reusable and single-use options. Their product line includes conventional, fiber optic, and LED-enhanced blades (such as Macintosh and Miller types) as well as reusable airway tube forceps. These devices are designed for airway management in clinical settings.
Where is Maco International based, and where are their devices primarily used?
Maco International is based in the United States. Their devices are intended for use in the U.S. market, where they must comply with applicable medical device regulations, including FDA requirements.
Which regulatory registries list Maco International’s devices?
Maco International’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices authorized for use in the U.S., ensuring transparency and traceability.
How are Maco International’s devices classified under FDA regulations?
Maco International’s devices fall under Class I classification according to FDA regulations. This classification applies to low-risk devices that pose minimal potential harm to users, though they still must meet compliance standards for safety and performance.
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
- 152941683
Catalogue (137)
Page 1 of 3| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Conventional Laryngoscope Handle | 7860 | FDA UDI | Class I | Active |
| Dispoasble Fiber Optic Laryngoscope Blade | 5060 | FDA UDI | Class I | Active |
| Macintosh (A) LED Blade | LA4462-1 | FDA UDI | Class I | Active |
| Macintosh (E) LED Blade | LE4462-14 | FDA UDI | Class I | Active |
| Macintosh (E) Blade | E4462-13 | FDA UDI | Class I | Active |
| Miller (A) LED Blade | LA6226-00 | FDA UDI | Class I | Active |
| Dispoasble Fiber Optic Laryngoscope Blade | 6060 | FDA UDI | Class I | Active |
| Macintosh FO German Blade | FO2311 | FDA UDI | Class I | Active |
| Miller FO German Blade | FO2410 | FDA UDI | Class I | Active |
| Macintosh (A) LED Blade | LA4462-3 | FDA UDI | Class I | Active |
| Disposable Conventional Laryngoscope Blade | 7060 | FDA UDI | Class I | Active |
| Miller (A) LED Blade | LA6226-1 | FDA UDI | Class I | Active |
| Macintosh FO (A) Detachable Blade | FO4312 | FDA UDI | Class I | Active |
| Miller (E) Blade | E6226-13 | FDA UDI | Class I | Active |
| Macintosh FO (E) Detachable Blade | FO6112 | FDA UDI | Class I | Active |
| Wisconsin Blade | 8662-1 | FDA UDI | Class I | Active |
| Macintosh (E) LED Blade | LE4462-12 | FDA UDI | Class I | Active |
| Wisconsin LED Blade | L8662-0 | FDA UDI | Class I | Active |
| Miller (A) LED Blade | LA6226-4 | FDA UDI | Class I | Active |
| Macintosh (A) Blade | A4462-2 | FDA UDI | Class I | Active |
| Dispoasble Fiber Optic Laryngoscope Blade | 60600 | FDA UDI | Class I | Active |
| Miller (E) LED Blade | LE6226-10 | FDA UDI | Class I | Active |
| Miller FO Detachable Blade | FO5224 | FDA UDI | Class I | Active |
| Disposable Conventional Laryngoscope Handle | D7862 | FDA UDI | Class I | Active |
| Miller (A) Blade | A6226-1 | FDA UDI | Class I | Active |
| Macintosh (E) Blade | E4462-12 | FDA UDI | Class I | Active |
| Wisconsin LED Blade | L8662-3 | FDA UDI | Class I | Active |
| Miller FO Detachable Blade | FO5221.5 | FDA UDI | Class I | Active |
| Macintosh (E) Blade | E4462-10 | FDA UDI | Class I | Active |
| Miller (E) LED Blade | LE6226-14 | FDA UDI | Class I | Active |
| Disposable Conventional Laryngoscope Blade | 7064 | FDA UDI | Class I | Active |
| Dispoasble Fiber Optic Laryngoscope Blade | 6063 | FDA UDI | Class I | Active |
| Phillips LED Blade | L8225-0 | FDA UDI | Class I | Active |
| Wisconsin Blade | 8662-4 | FDA UDI | Class I | Active |
| Macintosh (A) Blade | A4462-3 | FDA UDI | Class I | Active |
| Miller (A) Blade | A6226-00 | FDA UDI | Class I | Active |
| Macintosh FO (E) Detachable Blade | FO6113 | FDA UDI | Class I | Active |
| Dispoasble Fiber Optic Laryngoscope Blade | 5063 | FDA UDI | Class I | Active |
| Miller (E) Blade | E6226-14 | FDA UDI | Class I | Active |
| Wisconsin LED Blade | L8662-1 | FDA UDI | Class I | Active |
| Dispoasble Fiber Optic Laryngoscope Blade | 5064 | FDA UDI | Class I | Active |
| Miller (E) Blade | E6226-100 | FDA UDI | Class I | Active |
| Conventional Laryngoscope Handle | 7961 | FDA UDI | Class I | Active |
| Macintosh FO German Blade | FO2314 | FDA UDI | Class I | Active |
| Disposable Conventional Laryngoscope Blade | 6042 | FDA UDI | Class I | Active |
| Macintosh FO (A) Detachable Blade | FO4311 | FDA UDI | Class I | Active |
| Macintosh (E) LED Blade | LE4462-11 | FDA UDI | Class I | Active |
| Wisconsin Blade | 8662-3 | FDA UDI | Class I | Active |
| Dispoasble Fiber Optic Laryngoscope Blade | 5061 | FDA UDI | Class I | Active |
| Wisconsin LED Blade | L8662-4 | FDA UDI | Class I | Active |
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