Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K003695Substantially Equivalent

Microscope-Stainless Steel/fiber Optic: .5-2.6Mm Model Mmd 4500 Series and 2.7-5.0Mm Model Mmd-4700 Series

Micro Medical Devices, Inc., Cleveland OH / Traditional, Substantially Equivalent

K003695 is the FDA 510(k) clearance record for MICROSCOPE-STAINLESS STEEL/FIBER OPTIC: .5-2.6MM MODEL MMD 4500 SERIES AND 2.7-5.0MM MODEL MMD-4700 SERIES, a class II device, cleared for Micro-Medical Devices, Inc. on under FDA product code HRX (Arthroscope). FDA's definition for product code HRX reads: "Validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission if the device is reusable and has specific design features (please refer to Table 2 of 82 FR 26807, available...". FDA records list 8 510(k) clearances for Micro-Medical Devices, Inc., from to . As of , FDA records show no recalls naming K003695.

Clearance record

Decision date
Received
(76 days to decision)
Product code
HRX Arthroscope
Regulation
21 CFR 888.1100
Device class
Class II
Review panel
Orthopedic
Applicant
Micro-Medical Devices, Inc. 11000 Cedar Ave., Cleveland OH
510(k) summary
Summary
Third party review
No

Clearances, product code HRX

Trailing 12 months
9 clearances under product code HRX in the twelve months to October 2026, November 2025 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code HRX, trailing twelve months
MonthClearances
November 20252
December 20252
January 20260
February 20260
March 20261
April 20261
May 20261
June 20260
July 20260
August 20262
September 20260
October 20260