510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K203472Substantially Equivalent

KMTI Hip Replacement System

Kyocera Medical Technologies, Inc., Redlands CA / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K203472 is the FDA 510(k) clearance record for KMTI Hip Replacement System, a class II device, cleared for Kyocera Medical Technologies, Inc. on under FDA product code OQG (Hip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, Uncemented). FDA's definition for product code OQG reads: "1. Non-inflammatory degenerative joint disease including osteoarthritis and avascular necrosis. 2. Rheumatoid arthritis. 3. Correction of functional deformity. 4. Treatment of non-union, femoral neck fracture, and trochanteric fractures of...". FDA records list 16 510(k) clearances for Kyocera Medical Technologies, Inc., from to . As of , FDA records show no recalls naming K203472.

Clearance record

Decision date
Received
(128 days to decision)
Product code
OQG Hip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, Uncemented
Regulation
21 CFR 888.3358
Device class
Class II
Review panel
Orthopedic
Applicant
Kyocera Medical Technologies, Inc. 1200 California St., Redlands CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code OQG

Trailing 12 months

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

FDA records show no clearances under product code OQG in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code OQG, 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