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META 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
LinkedIn
—
Facebook
—
Phone
+390522502311
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
442368394

Catalogue (7)

DeviceModel / ReferenceRegistriesClassStatus
Safescraper Twist curve Volumizer 5501
FDA UDI
Class IActive
Safescraper Twist 3598
FDA UDI
Class IActive
Smartscraper 4890
EUDAMEDFDA UDI
Class IActive
Safescraper Twist 5532
FDA UDI
Class IActive
Safescraper Twist Curve Volumizer 5535
EUDAMEDFDA UDI
Class IActive
Safescraper Twist Curve 5530
EUDAMEDFDA UDI
Class IActive
Micross Curve 5542
EUDAMEDFDA UDI
Class IActive

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