510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K003612Substantially Equivalent

Microspeed Ec Motorsystem Gd650/gd653

Aesculap Inc, Center Valley PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K003612 is the FDA 510(k) clearance record for MICROSPEED EC MOTORSYSTEM GD650/GD653, a class II device, cleared for Aesculap, Inc. on under FDA product code HBC (Motor, Drill, Electric). FDA records list 269 510(k) clearances for Aesculap, Inc., from to . As of , FDA records show no recalls naming K003612.

Clearance record

Decision date
Received
(90 days to decision)
Product code
HBC Motor, Drill, Electric
Regulation
21 CFR 882.4360
Device class
Class II
Review panel
Neurology
Applicant
Aesculap, Inc. 3773 Executive Center Pkwy., Center Valley PA
510(k) summary
Summary
Third party review
No

Clearances, product code HBC

Trailing 12 months
1 clearance under product code HBC in the twelve months to November 2026, September 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code HBC, trailing twelve months
MonthClearances
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20261
October 20260
November 20260