ClearanceBrief
Company ยท US

Osteogenics, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1996 to 2007. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
FTLMesh, Surgical, Polymeric2
GXPMethyl Methacrylate For Cranioplasty2
LYCBone Grafting Material, Synthetic2

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jul 17, 2007K061934XTAC
Osteogenics, Inc.
FTL
Nov 18, 1999K983753STAR TEMPORARY WOUND COVER
Osteogenics, Inc.
FTL
Aug 6, 1997K972278CYTOPLAST REGENTEX TITANIUM 250
Osteogenics Co.
LYC
Mar 11, 1997K964342CYTOPLAST GBR
Osteogenics Co.
LYC
Jan 24, 1997K964537BONESOURCE HYDROXYAPATITE CEMENT (HAC)
Osteogenics, Inc.
GXP
Jun 27, 1996K953339BONESOURCE HYDROXYAPATITE CEMENT (HAC)
Osteogenics, Inc.
GXP

Latest recalls

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