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by
Innolitics
Anesthesiology
Review Panel
Cardiovascular
Review Panel
Chemistry
Review Panel
Dental
Review Panel
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Review Panel
Gastroenterology and Urology
Review Panel
General Hospital
Review Panel
Hematology
Review Panel
Immunology
Review Panel
Microbiology
Review Panel
Neurology
Review Panel
Obstetrical and Gynecological
Review Panel
Ophthalmic
Review Panel
Miscellaneous
Miscellaneous
Subpart B—Diagnostic Devices
CFR Sub-Part
Subpart D—Prosthetic Devices
CFR Sub-Part
HPZ
Implant, Eye Sphere
2
Product Code
HQH
Eye, Artificial, Non-Custom
1
Product Code
HQJ
Implant, Absorbable, (Scleral Buckling Methods)
2
Product Code
HQL
Intraocular Lens
3
Product Code
HQM
Keratoprosthesis, Permanent Implant
2
Product Code
HQN
Conformer, Ophthalmic
2
Product Code
HQT
Shell, Scleral
2
Product Code
HQW
Clip, Tantalum, Ophthalmic
2
Product Code
HQX
Implant, Orbital, Extra-Ocular
2
Product Code
K
02
3481
MICROVISION SCLERAL BUCKLING COMPONENTS
2
Cleared 510(K)
K
98
3581
OCU-GUARD AND OCU-GUARD SUPPLE
2
Cleared 510(K)
K
98
0816
RETINAL DETACHMENT IMPLANTS, INCLUDING BANDS, STRIPS (RAILS) AND SPONGES
2
Cleared 510(K)
K
96
3219
RETINAL DETACHMENT IMPLANTS; INCLUDING BANS, STRIPS, TIRES, SLEEVES, CORDS AND SPONGES
2
Cleared 510(K)
K
95
0806
SOLID DILICONE IMPLANTS, SDILICONE SPONGE IMPLANTS
2
Cleared 510(K)
K
95
0599
STORS SCLERAL SPONGE II (LINCOFF DESIGN)
2
Cleared 510(K)
K
94
5172
VISITEC SILICONE RETINAL IMPLANTS/EXPLANTS
2
Cleared 510(K)
K
90
2308
TAMCENAN OCULAR EXPLANTS AND BANDS
2
Cleared 510(K)
K
90
1002
O'DONNELL, SOCKET RECONSTRUCTION PROSTHESES
2
Cleared 510(K)
K
90
0929
PUTTERMAN-SCOTT, SOCKET RECONSTRUCTION BILATERAL
2
Cleared 510(K)
K
90
0930
SPIVEY-ALLEN ORBITAL FLOOR IMPLANT
2
Cleared 510(K)
K
90
0928
COX MALAR EMINENCE IMPLANTS
2
Cleared 510(K)
K
90
0927
CODERE-DURETTE ORBITAL FLOOR IMPLANT
2
Cleared 510(K)
K
86
3946
POREX(TM) EXTRA-OCULAR ORBITAL IMPLANT
2
Cleared 510(K)
K
83
2481
SCLERAL BUCKLING IMPLANTS DIF/TYPES
2
Cleared 510(K)
K
80
0140
SILASTIC SCLERAL SPONGE II W/CIRCLING BD
2
Cleared 510(K)
KYF
Implant, Eye Valve
2
Product Code
MFK
Lens, Multifocal Intraocular
3
Product Code
MJP
Lens, Intraocular, Toric Optics
3
Product Code
MLP
Keratoprosthesis, Temporary Implant, Surgical Use
2
Product Code
MQU
Ocular Peg
2
Product Code
MTZ
Wrap, Implant, Orbital
2
Product Code
NAA
Lens, Intraocular, Accommodative
3
Product Code
NCK
Button, Iris, Eye, Artificial
1
Product Code
NFM
Expander, Tissue, Orbital
2
Product Code
NIZ
Lens, Iris Reconstruction
3
Product Code
NQB
Conformer, Ophthalmic, Biological Tissue
2
Product Code
NXM
Prosthesis, Eyelid Spacer/Graft, Biologic
2
Product Code
POE
Extended Depth Of Focus Intraocular Lens
3
Product Code
PUF
Ocular Peg, Exempt
2
Product Code
PZK
Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)
3
Product Code
QCB
Phakic Toric Intraocular Lens
3
Product Code
QWU
Prosthesis, Eyelid Spacer/Graft, Polymer
2
Product Code
Subpart E—Surgical Devices
CFR Sub-Part
Subpart F—General Hospital and Personal Use Therapeutic Devices
CFR Sub-Part
Subpart F—Therapeutic Devices
CFR Sub-Part
Orthopedic
Review Panel
Pathology
Review Panel
Physical Medicine
Review Panel
Radiology
Review Panel
General and Plastic Surgery
Review Panel
Toxicology
Review Panel
Medical Genetics
Review Panel
Unknown
Review Panel
Last synced on 9 May 2025 at 11:05 pm
OP
/
subpart-d—prosthetic-devices
/
HQX
/
K900928
View Source
COX MALAR EMINENCE IMPLANTS
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900928
510(k) Type
Traditional
Applicant
OCULO PLASTIK, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
5/15/1990
Days to Decision
77 days
FDA Browser
by
Innolitics
Anesthesiology
Cardiovascular
Chemistry
Dental
Ear, Nose, Throat
Gastroenterology and Urology
General Hospital
Hematology
Immunology
Microbiology
Neurology
Obstetrical and Gynecological
Ophthalmic
Miscellaneous
Subpart B—Diagnostic Devices
Subpart D—Prosthetic Devices
HPZ
Implant, Eye Sphere
HQH
Eye, Artificial, Non-Custom
HQJ
Implant, Absorbable, (Scleral Buckling Methods)
HQL
Intraocular Lens
HQM
Keratoprosthesis, Permanent Implant
HQN
Conformer, Ophthalmic
HQT
Shell, Scleral
HQW
Clip, Tantalum, Ophthalmic
HQX
Implant, Orbital, Extra-Ocular
K
02
3481
MICROVISION SCLERAL BUCKLING COMPONENTS
K
98
3581
OCU-GUARD AND OCU-GUARD SUPPLE
K
98
0816
RETINAL DETACHMENT IMPLANTS, INCLUDING BANDS, STRIPS (RAILS) AND SPONGES
K
96
3219
RETINAL DETACHMENT IMPLANTS; INCLUDING BANS, STRIPS, TIRES, SLEEVES, CORDS AND SPONGES
K
95
0806
SOLID DILICONE IMPLANTS, SDILICONE SPONGE IMPLANTS
K
95
0599
STORS SCLERAL SPONGE II (LINCOFF DESIGN)
K
94
5172
VISITEC SILICONE RETINAL IMPLANTS/EXPLANTS
K
90
2308
TAMCENAN OCULAR EXPLANTS AND BANDS
K
90
1002
O'DONNELL, SOCKET RECONSTRUCTION PROSTHESES
K
90
0929
PUTTERMAN-SCOTT, SOCKET RECONSTRUCTION BILATERAL
K
90
0930
SPIVEY-ALLEN ORBITAL FLOOR IMPLANT
K
90
0928
COX MALAR EMINENCE IMPLANTS
K
90
0927
CODERE-DURETTE ORBITAL FLOOR IMPLANT
K
86
3946
POREX(TM) EXTRA-OCULAR ORBITAL IMPLANT
K
83
2481
SCLERAL BUCKLING IMPLANTS DIF/TYPES
K
80
0140
SILASTIC SCLERAL SPONGE II W/CIRCLING BD
KYF
Implant, Eye Valve
MFK
Lens, Multifocal Intraocular
MJP
Lens, Intraocular, Toric Optics
MLP
Keratoprosthesis, Temporary Implant, Surgical Use
MQU
Ocular Peg
MTZ
Wrap, Implant, Orbital
NAA
Lens, Intraocular, Accommodative
NCK
Button, Iris, Eye, Artificial
NFM
Expander, Tissue, Orbital
NIZ
Lens, Iris Reconstruction
NQB
Conformer, Ophthalmic, Biological Tissue
NXM
Prosthesis, Eyelid Spacer/Graft, Biologic
POE
Extended Depth Of Focus Intraocular Lens
PUF
Ocular Peg, Exempt
PZK
Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)
QCB
Phakic Toric Intraocular Lens
QWU
Prosthesis, Eyelid Spacer/Graft, Polymer
Subpart E—Surgical Devices
Subpart F—General Hospital and Personal Use Therapeutic Devices
Subpart F—Therapeutic Devices
Orthopedic
Pathology
Physical Medicine
Radiology
General and Plastic Surgery
Toxicology
Medical Genetics
Unknown
OP
/
subpart-d—prosthetic-devices
/
HQX
/
K900928
View Source
COX MALAR EMINENCE IMPLANTS
Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900928
510(k) Type
Traditional
Applicant
OCULO PLASTIK, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
5/15/1990
Days to Decision
77 days