510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K914960Substantially Equivalent

Instrument Organizer

O.R. Concepts, Inc., Roanoke TX / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K914960 is the FDA 510(k) clearance record for INSTRUMENT ORGANIZER, a class I device, cleared for O.R. Concepts, Inc. on under FDA product code KDC (Instrument, Surgical, Disposable). FDA records list 34 510(k) clearances for O.R. Concepts, Inc., from to . As of , FDA records show no recalls naming K914960.

Clearance record

Decision date
Received
(115 days to decision)
Product code
KDC Instrument, Surgical, Disposable
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
O.R. Concepts, Inc. 200 N. Oak St., Roanoke TX
510(k) summary
Statement
Third party review
No

Clearances, product code KDC

Trailing 12 months

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

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