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Dark Star Deformity 100257

by Republic Spine, LLC

Dark Star Deformity 100257 (DS0027) is a Class II device made by Republic Spine, LLC, listed in FDA GUDID since 18 Nov 2025 (UDI-DI B0751002570), 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 NumberB0751002570 UDI-DI Date18 Nov 2025ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Dark Star Deformity
Generic name
Abdominal/ENT/orthopaedic surgical probe, reusable
Model / Ref / Catalog
100257, DS0027
Primary DI / UDI-DI
B0751002570
FDA product code
MNI, MNH
GMDN term
Abdominal/ENT/orthopaedic surgical probe, reusable
Device class
Class II
Regulation number
888.3070
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
MRI safety
MR Unsafe

Other devices from Republic Spine, LLC

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Properties

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