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Sign in to claim this brandDevroye Instruments Belgium
US
Last updated May 30, 2026
What Devroye Instruments Belgium makes
Devroye Instruments Belgium manufactures hair extraction punches, including reusable electrosurgical handpieces designed for precise tissue removal, and associated software for procedural support. The product line includes various punch sizes and a support box for compatibility with electrosurgical systems.
These devices are classified as Class I under regulatory frameworks, with product listings maintained in the FDA’s Unique Device Identifier (UDI) database. The company operates from Belgium, though its devices are authorised for use in the US market.
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 Devroye Instruments Belgium manufacture?
Devroye Instruments Belgium specialises in hair extraction punches, which are tools used for precise tissue removal, and reusable electrosurgical handpieces designed to work with electrosurgical systems. Their product line also includes software that supports procedural workflows. These devices are primarily used in medical settings where controlled tissue extraction is required.
Where is Devroye Instruments Belgium based, and where are their devices authorised for use?
Devroye Instruments Belgium is based in Belgium, though their devices are authorised for use in the US market. The company’s products are designed and manufactured in compliance with relevant regulatory standards, enabling them to be legally marketed and used in the United States.
Which regulatory registries list Devroye Instruments Belgium’s devices?
Devroye Instruments Belgium’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency of medical devices authorised for use in the US, including their specific identifiers and classifications.
How are Devroye Instruments Belgium’s devices classified under regulatory frameworks?
Devroye Instruments Belgium’s devices are classified as Class I under regulatory frameworks. This classification applies to products that pose minimal risk to patients and users, often due to their low-risk nature or non-invasive use. Class I devices typically require less stringent regulatory oversight compared to higher-risk categories.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- devroyeinstruments.com
- —
- —
- [email protected]
- Phone
- +3208807064
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 372521769
Catalogue (12)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| WAW HYBRID TORNADO Schambach PUNCH 1.00 | 1.00LH2508 | FDA UDI | Class I | Active |
| Waw Hybrid Tornado Punch 1.20 | 1.202508 | FDA UDI | Class I | Active |
| Punch Support Box | 1 | FDA UDI | Class I | Active |
| Waw Hybrid Tornado Punch 1.05 | 1.052508 | FDA UDI | Class I | Active |
| Waw Hybrid Tornado Punch 0.80 | 0.802508 | FDA UDI | Class I | Active |
| Waw Hybrid Tornado Punch 0.95 | 0.952508 | FDA UDI | Class I | Active |
| Waw Hybrid Tornado Punch 0.85 | 0.852508 | FDA UDI | Class I | Active |
| Waw Hybrid Tornado Punch 1.10 | 1.102508 | FDA UDI | Class I | Active |
| Waw Hybrid Tornado Punch 0.90 | 0.902508 | FDA UDI | Class I | Active |
| Waw Hybrid Tornado Punch 1.00 | 1.002508 | FDA UDI | Class I | Active |
| Waw Software | 0.1.35 | FDA UDI | Class I | Active |
| WAW HYBRID TORNADO Schambach PUNCH | 1.00LH2407 | FDA UDI | Class I | Active |
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