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
K200977Substantially Equivalent

Modular Toga

Operating Room Innovations, Inc, San Diego CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K200977 is the FDA 510(k) clearance record for Modular Toga, a class II device, cleared for Operating Room Innovations, Inc. on under FDA product code FYA (Gown, Surgical). FDA records list one 510(k) clearance for Operating Room Innovations, Inc. As of , FDA records show no recalls naming K200977.

Clearance record

Decision date
Received
(114 days to decision)
Product code
FYA Gown, Surgical
Regulation
21 CFR 878.4040
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Operating Room Innovations, Inc. 5694 Mission Center Rd. Suite 602, San Diego CA
510(k) summary
Statement
Third party review
No

Clearances, product code FYA

Trailing 12 months
10 clearances under product code FYA in the twelve months to October 2026, February 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code FYA, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20262
March 20260
April 20262
May 20261
June 20261
July 20261
August 20262
September 20260
October 20260