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Zuga MRA-500-360

by Zuga Medical, Inc.

Zuga MRA-500-360 is a dental implant suprastructure (FDA Class I; FDA product code NDP, Accessories, Implant, Dental, Endosseous) made by Zuga Medical, Inc., listed in FDA GUDID since 15 Jan 2018 (UDI-DI 00854382006729), 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 Number00854382006729 UDI-DI Date15 Jan 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  • Withdrawn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
Zuga
Generic name
Dental implant suprastructure, temporary, preformed, single-use
Model / reference
MRA-500-360
Primary DI / UDI-DI
00854382006729
FDA product code
NDP
GMDN term
Dental implant suprastructure, temporary, preformed, single-use
Device class
Class I
Regulation number
872.3980
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Dental implant suprastructure, temporary, preformed, single-use

Similar devices in this category

Other devices filed under Dental implant suprastructure, temporary, preformed, single-use.

Other devices from Zuga Medical, Inc.

  • Zuga ZTK-000-000

    Class II

  • Zuga TRK-350-055

    Class II

  • Zuga TAA-500-470

    Class II

  • Zuga GST-350-000

    Class II

See all devices from Zuga Medical, Inc. →

Properties

  • Sterilise before use
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (9, all answered No)