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G21 SRL

Country not established

G21 SRL is a medical device manufacturer, with 94 devices listed in FDA GUDID and EUDAMED (FDA Class II and I) as of 13 Nov 2026.

Devices
94

Registry facts

Counted by deviCERTS from registry records, 13 Nov 2026

Registries
  • FDA GUDID 94
  • EUDAMED 7

A device listed in two registries counts in both.

Device classes
  • FDA Class II 56
  • FDA Class I 38
Identifiers
  • DUNS 431529195

What G21 SRL makes

G21 SRL manufactures orthopaedic devices for spinal and bone procedures, including moulds for cement spacers, balloon kyphoplasty kits for vertebral augmentation, and kits for preparing and delivering orthopaedic cement. Their portfolio also includes antimicrobial and non-antimicrobial bone cement, cannulae for vertebral body cement injection, bone access channel kits, and reusable surgical procedure kits for orthopaedic use.

The company’s devices are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database. G21 SRL operates from the United States, adhering to applicable regulatory requirements for medical devices in that jurisdiction.

AI-generated from registry data, 19 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue94

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Company details

DUNS number
431529195

Frequently asked questions

How many devices does G21 SRL have in the registry?

The registry currently lists 94 devices for G21 SRL. Devices recorded under merged duplicate company entries are counted once.

Which registries list G21 SRL's devices?

Among its 50 most recently registered devices, G21 SRL has devices listed in EUDAMED (3 devices) and FDA GUDID (50 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do G21 SRL's devices fall under?

Among its 50 most recently registered devices, the classes recorded for G21 SRL's devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from G21 SRL in the registry?

The most recently registered devices listed for G21 SRL include KeyFix Direct Access Needle Trocar and bevel tip, 13 gauge 900106, Easy Winch 13 G, 15 mm 900222, Easy Winch 13 G, 10 mm 900221 and Winch Kyphoplasty Balloon Catheter 15G 10 mm 900025.

Generated automatically from registry data and not verified by a human reviewer.