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Actifuse Shape 506005078068

by Apatech Ltd

Actifuse Shape 506005078068 is a Class II device made by Apatech Ltd, listed in FDA GUDID since 24 Sep 2015 (UDI-DI 05060050780685), 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 Number05060050780685 UDI-DI Date24 Sep 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  • Withdrawn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
Actifuse Shape
Generic name
Orthopaedic bone void filling material, synthetic, bioabsorbable, non-antimicrobial
Model / Ref / Catalog
506005078068
Primary DI / UDI-DI
05060050780685
FDA product code
LYC, MQV
GMDN term
Orthopaedic bone void filling material, synthetic, bioabsorbable, non-antimicrobial
Device class
Class II
Regulation number
872.3930, 888.3045
GUDID distribution status
In Commercial Distribution
Size
Total Volume — 15.8 Milliliter

Related devices

Category: Bone matrix implant, synthetic, non-antimicrobial

Similar devices

Other devices filed under FDA product code LYC (Bone grafting material, synthetic).

Other devices from Apatech Ltd

See all devices from Apatech Ltd →

Properties

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