ClearanceBrief
Company ยท US

Innova Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 1991 to 2004. 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
DZEImplant, Endosseous, Root-Form4
LYGMassager, Therapeutic, Manual1
MQNExternal Mandibular Fixator And/Or Distractor1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Apr 9, 2004K040714HYBRID ENDOPORE ENDOSSEOUS DENTAL IMPLANT
Innova Corp.
DZE
Feb 10, 1999K984117INNOVA TELESCOPIC DISTRACTOR
Innova Corp.
MQN
May 8, 1997K971196ENDOPORE ENDOSSEOUS DENTAL IMPLANT SYSTEM
Innova Corp.
DZE
Jul 19, 1995K952434ENDOPORE DENTAL IMPLANT ABUTMENTS
Innova Corp.
DZE
Feb 13, 1995K926354ENDO-PORE ENDOSSEOUS DENTAL IMPLANT SYSTEM
Innova Corp.
DZE
Dec 20, 1991K915361THE BODY BUGGY
Innova Corp.
LYG

Latest recalls

DateFirm and productCodeLinked 510(k)
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