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Sign in to claim this brandMETA TECHNOLOGIES SRL
US
Last updated May 30, 2026
What META TECHNOLOGIES SRL makes
META TECHNOLOGIES SRL manufactures bone collection scrapers designed for surgical procedures, including curved and twist-style variants for precise tissue removal. Their product line includes devices like the Safescraper Twist Curve Volumizer, Smartscraper, and Micross Curve, which are intended for use in orthopedic and reconstructive surgeries.
These devices are classified under Class I in the FDA’s regulatory framework and are listed in the FDA’s Unique Device Identifier (UDI) database. The company 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 Meta Technologies SRL manufacture?
Meta Technologies SRL specializes in bone collection scrapers, which are surgical tools used to remove tissue during procedures. Their product line includes devices like the Safescraper Twist Curve Volumizer, Smartscraper, and Micross Curve, designed for precision in orthopedic and reconstructive surgeries. These tools are engineered to assist surgeons in controlled tissue removal, ensuring efficiency and safety during operations.
Where is Meta Technologies SRL based?
Meta Technologies SRL is headquartered in the United States. The company’s location in the US aligns with its focus on manufacturing and distributing medical devices that comply with regional regulatory standards, including those of the FDA.
Which regulatory registries list Meta Technologies SRL’s devices?
Meta Technologies SRL’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency in the medical device supply chain, allowing healthcare providers and regulators to verify product details and compliance information.
How are Meta Technologies SRL’s devices classified under FDA regulations?
Meta Technologies SRL’s bone collection scrapers fall under Class I classification in the FDA’s regulatory framework. Class I devices are generally considered low-risk and typically require less stringent premarket review, though they must still meet safety and performance standards to ensure proper use in surgical settings.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- metahosp.com
- —
- —
- [email protected]
- Phone
- +390522502311
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 442368394
Catalogue (7)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Safescraper Twist curve Volumizer | 5501 | FDA UDI | Class I | Active |
| Safescraper Twist | 3598 | FDA UDI | Class I | Active |
| Smartscraper | 4890 | EUDAMEDFDA UDI | Class I | Active |
| Safescraper Twist | 5532 | FDA UDI | Class I | Active |
| Safescraper Twist Curve Volumizer | 5535 | EUDAMEDFDA UDI | Class I | Active |
| Safescraper Twist Curve | 5530 | EUDAMEDFDA UDI | Class I | Active |
| Micross Curve | 5542 | EUDAMEDFDA UDI | Class I | Active |
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