FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

BIOCERAMIC ORBITAL IMPLANT

K Number: K992294 · Decision Apr 19, 2000
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
38
Applicant Total
13
Review Days
287

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Basic Information

Device Name
BIOCERAMIC ORBITAL IMPLANT
K Number
K992294
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.3320
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Fci Ophthalmics, Inc.
Date Received
July 7, 1999
Decision Date
April 19, 2000
Product Code
HPZ
Advisory Committee
Ophthalmic
Review Advisory Committee
OP
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HPZ Implant, Eye Sphere

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HPZ), ordered by most recent decision date.

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Other Clearances by Fci Ophthalmics, Inc.

K Number Device Name
K061404 MONO-CRAWFORD NASO-LACRIMAL INTUBATION DEVICE
K061398 SNUG PLUG PUNCTUM PLUG
K041869 SELF RETAINING BICANALICULUS INTUBATION SET
K023758 BECKER TRANSNASAL LACRIMAL (INTUBATION SETS)
K023400 FCI MESH WRAPPED BIOCERAMIC ORBITAL IMPLANT
K030054 DISPOSABLE VITRECTOMY SETS, DISPOSABLE VIRECTOMY LENSES
K991238 FCI CRAWFORD PROBE INTUBATION SETS
K980816 RETINAL DETACHMENT IMPLANTS, INCLUDING BANDS, STRIPS (RAILS) AND SPONGES
K980822 TITANIUM PEG SYSTEM
K964774 PUNCTUM PLUGS & READY-SET PUNCTAL PLUGS
Search all 13 clearances from Fci Ophthalmics, Inc. →