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M4412 Magic Motion

by InnoBioSurg Co., Ltd(IBS implant Co., Ltd) GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08800039307062 UDI-DIDate8 Nov 2018ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 23 Oct 2026.

Specification

GUDID

Trade Name
M4412
Generic Name
Screw endosteal dental implant, two-piece
Model / Reference
Magic Motion
Primary DI / UDI-DI
08800039307062
510(k) Number
FDA Product Code
NHA, DZE
GMDN Term
Screw endosteal dental implant, two-piece
Device Class
Class II
Regulation Number
872.3630, 872.3640
GUDID distribution status
In Commercial Distribution

Related devices

Category: Screw endosteal dental implant, two-pieceDental implant systemScrew endosteal dental implant, one-piece

Cleared under the same submission (K162099)

Show all (12)

Other devices from InnoBioSurg Co., Ltd(IBS implant Co., Ltd)

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Properties

  • Single Use
  • Implantable
  • Lot / Batch Number
  • Serial Number
  • Expiration Date
  • Manufacturing Date

Other properties (8)

  • Sterile: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No