ClearanceBrief
Company ยท US

Biomaterials Korea, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2007 to 2023. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
OATImplant, Endosseous, Orthodontic4
JEYPlate, Bone1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Aug 21, 2023K222245ACR Screw System
Biomaterials Korea, Inc., KR
OAT
Aug 30, 2018K173623Anchor plate
Biomaterials Korea, Inc., KR
OAT
Dec 8, 2011K110926BONE PLATE; BONE SCREW
Biomaterials Korea, Inc.
JEY
Sep 26, 2011K111809SL TYPE ORTHODONTIC ANCHOR SCREWS, SPL TYPE ORTHODONTIC ANCHOR SCREWS
Biomaterials Korea, Inc.
OAT
Jul 26, 2007K063495C TYPE, CT TYPE, AND SPECIAL TYPE ORTHODONTIC ANCHOR SCREWS
Biomaterials Korea, Inc.
OAT

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
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