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Endcap Universal 1813-00-005

by Biomet Orthopedics, Inc.

Endcap Universal 1813-00-005 (181300005) is a Class II device made by Biomet Orthopedics, Inc., listed in FDA GUDID since 24 Oct 2015 (UDI-DI 00887868019234), 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 Number00887868019234 UDI-DI Date24 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  • Withdrawn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
Endcap Universal
Generic name
Bone nail implantable cap
Model / Ref / Catalog
1813-00-005, 181300005
Primary DI / UDI-DI
00887868019234
FDA product code
KTT, HRS, LXT, HWC, JDW, HTN, HTY, HSB
GMDN term
Bone nail implantable cap
Device class
Class II
Regulation number
888.3030, 888.3040, 888.3020
GUDID distribution status
In Commercial Distribution

Related devices

Category: Bone nail end-cap

Other devices from Biomet Orthopedics, Inc.

See all devices from Biomet Orthopedics, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)