Anthem 2181.7308

by Globus Medical, Inc.

Anthem 2181.7308 is a Class II device made by Globus Medical, Inc., listed in FDA GUDID since 25 Nov 2021 (UDI-DI 00193982355111), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00193982355111 UDI-DI	Date25 Nov 2021Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00193982355111

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Anthem
Generic name: Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile
Model / reference: 2181.7308

Primary DI / UDI-DI: 00193982355111
FDA product code: HWC, HRS
GMDN term: Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile

Device class: Class II
Regulation number: 888.3040, 888.3030
GUDID distribution status: In Commercial Distribution

Sterilisation method: Moist Heat or Steam Sterilization

Similar devices in this category

Other devices filed under Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile.

Other devices from Globus Medical, Inc.

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Properties

Sterilise before use
Single use
Lot / batch number

Other properties (12, all answered No)