Metapaste Plus
K-Number: K210904 · 2021-06-30
ApplicantMeta Biomed Co., Ltd.
Decision Date2021-06-30
Product CodeKIF
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Metapaste Plus is a medical device manufactured by Meta Biomed Co., Ltd.. It received FDA 510(k) clearance on 2021-06-30 under approval number K210904. The device is classified under product code KIF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Metapaste Plus?
Metapaste Plus is a medical device that received FDA 510(k) clearance on 2021-06-30. It is manufactured by Meta Biomed Co., Ltd.. The 510(k) number is K210904.
When was Metapaste Plus approved by the FDA?
Metapaste Plus received FDA 510(k) clearance on 2021-06-30, under approval number K210904.
What company makes Metapaste Plus?
Metapaste Plus is manufactured by Meta Biomed Co., Ltd..
What is the FDA product code for Metapaste Plus?
The FDA product code for Metapaste Plus is KIF.
Other Devices by Meta Biomed Co., Ltd.
Related Devices (Code: KIF)
K161239MTA2.2 MATERIALAvalon Biomed, Inc.
K151047MTA Repair HPAngelus Industria DE Productos Odontologicos
K153067Tubli-Seal, Tubli-Seal EWT,Tubli-Seal Xpress, Tubli-Seal EWT XpressSybron Dental Specialties
K152956Pulp Canal Sealer, Pulp Canal Sealer EWTSybron Dental Specialties
K152959Sealapex tubes, Sealapex bulk package, Sealapex Xpress dual-barrel syringesSybron Dental Specialties
K170950Well-Root STVericom Co., Ltd.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.