MQU · Class II · 21 CFR 886.3320

FDA Product Code MQU: Ocular Peg

Leading manufacturers include Integrated Orbital Implants, Inc., Porex Technologies Corp. and Fci Ophthalmics, Inc..

4
Total
4
Cleared
89d
Avg days
1997
Since

FDA 510(k) Cleared Ocular Peg Devices (Product Code MQU)

4 devices
1–4 of 4
Cleared Apr 10, 2000
PERRY-KOLBERG (PK) HA-COATED TITANIUM SLEEVE
K000151
Integrated Orbital Implants, Inc.
Ophthalmic · 82d
Cleared Jul 09, 1998
TITANIUM PEG SYSTEM
K980822
Fci Ophthalmics, Inc.
Ophthalmic · 128d
Cleared Feb 04, 1998
PERRY-KOLBERG (PK) TITANIUM MOTILITY/SUPPORT SYSTEM
K974203
Integrated Orbital Implants, Inc.
Ophthalmic · 86d
Cleared Jun 30, 1997
MEDPOR OCULAR SCREW AND ACCEOSSORIES
K971583
Porex Technologies Corp.
Ophthalmic · 61d

About Product Code MQU - Regulatory Context