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Amii Implant 401M3013S

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

Amii Implant 401M3013S is a Class II device made by InnoBioSurg Co., Ltd(IBS implant Co., Ltd), cleared under FDA 510(k) K220079 on 14 Dec 2022 and listed in FDA GUDID since 23 Apr 2025 (UDI-DI 08809986615053), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

510(k) K220079

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08809986615053 UDI-DI Date23 Apr 2025ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK220079 Date14 Dec 2022DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K220079 decided 14 Dec 2022 Active
  • FDA GUDID UDI-DI 08809986615053 listed 23 Apr 2025 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K220079
  2. Listed FDA GUDID 08809986615053

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Amii Implant
Generic name
Dental implant system
Model / reference
401M3013S
Primary DI / UDI-DI
08809986615053
510(k) Number
FDA product code
DZE
GMDN term
Dental implant system
Device class
Class II
Regulation number
872.3640
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe

Similar devices in this category

Other devices filed under Dental implant system.

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Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Contains latex
  • Prescription use
  • Lot / batch number
  • Serial number
  • Expiration date
  • Manufacturing date
Other properties (6, all answered No)