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Proview 54-1050

by Orthofix US LLC

Proview 54-1050 is a Class I device made by Orthofix US LLC, listed in FDA GUDID since 17 Jul 2026 (UDI-DI 18257200051397), 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

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number18257200051397 UDI-DI Date17 Jul 2026ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Proview
Generic name
Surgical implant template, reusable
Model / reference
54-1050
Primary DI / UDI-DI
18257200051397
FDA product code
LXH
GMDN term
Surgical implant template, reusable
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution

Other devices from Orthofix US LLC

See all devices from Orthofix US LLC →

Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)