DEVICE: Bio-Eye® (00854066006083)
Device Identifier (DI) Information
Bio-Eye®
I0016P
In Commercial Distribution
INTEGRATED ORBITAL IMPLANTS INC
I0016P
In Commercial Distribution
INTEGRATED ORBITAL IMPLANTS INC
Perforated Coated Hydroxyapatite (HA) Orbital Implant & Conformer used for enucleations and eviscerations.
Device Characteristics
Labeling does not contain MRI Safety Information | |
No | |
No | |
Yes | |
Yes | |
No | |
Yes | |
No | |
No |
GMDN
[?]GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.
GMDN Term Code | GMDN Term Name | GMDN Term Definition | GMDN Term Status [?] | Implantable? |
---|---|---|---|---|
16065 | Ophthalmic conformer |
An ophthalmic device, typically constructed from moulded plastic, that is intended to be inserted temporarily between the eyeball and eyelid to maintain space in the orbital cavity and prevent closure or adhesions during the healing process following eye surgery. This is a single-use device.
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Active | false |
44477 | Orbital sphere implant wrap, non-biological |
An implantable ocular device designed as an external cover (a wrap) for an orbital implant used in enucleation surgery, and to protect the surrounding orbital tissue from the surface of the implant. It is typically made of materials available in sheet form [e.g., polylactide (PLA), hydroxyapatite] that can be cut to the desired shape and size. It may be made malleable by submersion in hot water, after which it can be formed to any three-dimensional (3-D) anatomical orientation. It will typically contain pores that allow for natural vascular tissue ingrowth.
|
Active | true |
46902 | Orbital sphere implant |
An implantable ocular device designed to permanently fill the orbital cavity following enucleation, evisceration, or after the removal of another ocular implant (used as a secondary implant), to replace the volume and possibly, given the surgical method, to impart motion to the eventual ocular prosthesis (the artificial eyeball). It is typically aspherical and may have porous surfaces to facilitate colonization by fibrovascular tissue to offer the advantages of reduced risk of infection or implant extrusion. It is available in various sizes and is typically made of polymethylmethacrylate (PMMA), poly 2-hydroxyethylmethacrylate (PHEMA), or silicone.
|
Active | true |
FDA Product Code
[?]Product Code | Product Code Name |
---|---|
HQN | Conformer, Ophthalmic |
MTZ | Wrap, Implant, Orbital |
HPZ | Implant, Eye Sphere |
FDA Premarket Submission
FDA Premarket Submission Number [?] | Supplement Number [?] |
---|---|
K003338 | 000 |
Sterilization
Storage and Handling
[?]Storage and Handling |
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No storage/handling found |
Clinically Relevant Size
[?]Size Type Text |
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Outer Diameter: 16 Millimeter |
Device Record Status
c922f097-6f8b-4f82-9985-f44c023b53f5
December 04, 2020
5
December 01, 2015
December 04, 2020
5
December 01, 2015
Alternative and Additional Identifiers Additional Identifiers
Package DI
[?]Package DI Number | Quantity per Package | Contains DI Package | Package Discontinue Date | Package Status | Package Type |
---|---|---|---|---|---|
No Package DIs found |
Secondary DI
[?]Issuing Agency [?] | Secondary DI Number |
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No Secondary DIs found |
Unit of Use DI
[?]
Unit of Use DI Number:
No Unit of Use DI Numbers Found
CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
[?]
1-800-424-6537
haimplants@ioi.com
haimplants@ioi.com