510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K791123Substantially Equivalent

Ear and Nose Specula

Xomed, Inc., Arnold MO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K791123 is the FDA 510(k) clearance record for EAR AND NOSE SPECULA, a class I device, cleared for Xomed, Inc. on under FDA product code EPY (Speculum, Ent). FDA records list 35 510(k) clearances for Xomed, Inc., from to . As of , FDA records show no recalls naming K791123.

Clearance record

Decision date
Received
(25 days to decision)
Product code
EPY Speculum, Ent
Regulation
21 CFR 878.1800
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Xomed, Inc. 1318 Lonedell Rd., Arnold MO
Third party review
No

Clearances, product code EPY

Trailing 12 months

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

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