Skip to content

Closed Knot Pusher 902813

by Biomet Orthopedics, Inc. 2 variants

Closed Knot Pusher 902813 is a Class I device made by Biomet Orthopedics, Inc., listed in FDA GUDID since 29 May 2023 (UDI-DI 00887868567490), 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 Number00887868567490 UDI-DI Date29 May 2023ListedStatusListed 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  • Withdrawn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
Closed Knot Pusher
Generic name
Suture knot pusher, reusable
Model / Ref / Catalog
902813
Primary DI / UDI-DI
00887868567490
FDA product code
HXO
GMDN term
Suture knot pusher, 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: Suture knot pusher, reusable

Similar devices in this category

Other devices filed under Suture knot pusher, reusable.

Other devices from Biomet Orthopedics, Inc.

See all devices from Biomet Orthopedics, Inc. →

Properties

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