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Ncb® 02.02155.048

by Zimmer, Inc.

Ncb® 02.02155.048 is a Class II device made by Zimmer, Inc., listed in FDA GUDID since 16 Oct 2015 (UDI-DI 00889024291515), 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 Number00889024291515 UDI-DI Date16 Oct 2015ListedStatusListed 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  • Withdrawn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
Ncb®
Generic name
Orthopaedic bone screw (non-sliding)
Model / Ref / Catalog
02.02155.048
Primary DI / UDI-DI
00889024291515
FDA product code
HWC, HRS
GMDN term
Orthopaedic bone screw (non-sliding)
Device class
Class II
Regulation number
888.3040, 888.3030
GUDID distribution status
In Commercial Distribution
MRI safety
MR Conditional

Related devices

Category: Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, sterile

Similar devices in this category

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

Other devices from Zimmer, Inc.

See all devices from Zimmer, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)