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Anterior Disc Prep 95-6989

by SeaSpine Orthopedics Corporation

Anterior Disc Prep 95-6989 is a Class I device made by SeaSpine Orthopedics Corporation, listed in FDA GUDID since 27 Mar 2020 (UDI-DI 10889981184537), 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 Number10889981184537 UDI-DI Date27 Mar 2020ListedStatusListed 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  • Withdrawn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
Anterior Disc Prep
Generic name
Scalpel handle, reusable
Model / Ref / Catalog
95-6989
Primary DI / UDI-DI
10889981184537
FDA product code
LXH
GMDN term
Scalpel handle, 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: Scalpel handle, reusable

Other devices from SeaSpine Orthopedics Corporation

See all devices from SeaSpine Orthopedics Corporation →

Properties

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