510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K974203Substantially Equivalent

Perry-Kolberg (Pk) Titanium Motility/support System

Integrated Orbital Implants Inc, San Diego CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K974203 is the FDA 510(k) clearance record for PERRY-KOLBERG (PK) TITANIUM MOTILITY/SUPPORT SYSTEM, a class II device, cleared for Integrated Orbital Implants, Inc. on under FDA product code MQU (Ocular Peg). FDA records list 5 510(k) clearances for Integrated Orbital Implants, Inc., from to . As of , FDA records show one recall naming K974203.

Clearance record

Decision date
Received
(86 days to decision)
Product code
MQU Ocular Peg
Regulation
21 CFR 886.3320
Device class
Class II
Review panel
Ophthalmic
Applicant
Integrated Orbital Implants, Inc. 4329 Graydon Rd., San Diego CA
510(k) summary
Summary
Third party review
No

Clearances, product code MQU

Trailing 12 months

FDA records hold no clearances under product code MQU in the trailing twelve months.

FDA records show no clearances under product code MQU in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code MQU, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260