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
K232435Substantially Equivalent

Rhinolaryngoscope system

Shenzhen Hugemed Medical Technical Development Co., Ltd, Shenzhen, CN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K232435 is the FDA 510(k) clearance record for Rhinolaryngoscope system, a class II device, cleared for Shenzhen HugeMed Medical Technical Development Co., Ltd. on under FDA product code EOB (Nasopharyngoscope (Flexible Or Rigid)). FDA's definition for product code EOB reads: "If the device is reusable, validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission (82 FR 26807, available at...". FDA records list 8 510(k) clearances for Shenzhen HugeMed Medical Technical Development Co., Ltd., from to . As of , FDA records show no recalls naming K232435.

Clearance record

Decision date
Received
(256 days to decision)
Product code
EOB Nasopharyngoscope (Flexible Or Rigid)
Regulation
21 CFR 874.4760
Device class
Class II
Review panel
Ear, Nose, Throat
Applicant
Shenzhen HugeMed Medical Technical Development Co., Ltd. 415, 416-1,516-1, Bldg. 2, # 1, Mawu Rd., Baoan, Shenzhen, CN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code EOB

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