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ReLine 10000310

by NuVasive, LLC

ReLine 10000310 is a Class I device made by NuVasive, LLC, listed in FDA GUDID since 24 Sep 2018 (UDI-DI 00887517475916), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00887517475916 UDI-DI Date24 Sep 2018ListedStatusListed 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  • Withdrawn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
ReLine
Generic name
Bone tap, reusable
Model / reference
10000310
Primary DI / UDI-DI
00887517475916
FDA product code
LXH
GMDN term
Bone tap, reusable
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Bone tap, reusable

Other devices from NuVasive, LLC

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    Class II

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    Class II

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    Class II

  • ReLine 3800240

    Class II

See all devices from NuVasive, LLC →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)