510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K983405Substantially Equivalent

Aceme Jupiter Scooter, 3-Wheeled, Model Jupiter 50

Aceme Technologies Intl., Sacramento CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K983405 is the FDA 510(k) clearance record for ACEME JUPITER SCOOTER, 3-WHEELED, MODEL JUPITER 50, a class II device, cleared for Aceme Technologies Intl. on under FDA product code INI (Vehicle, Motorized 3-Wheeled). FDA records list 2 510(k) clearances for Aceme Technologies Intl. As of , FDA records show no recalls naming K983405.

Clearance record

Decision date
Received
(39 days to decision)
Product code
INI Vehicle, Motorized 3-Wheeled
Regulation
21 CFR 890.3800
Device class
Class II
Review panel
Physical Medicine
Applicant
Aceme Technologies Intl. 5580 Power Inn Rd., Suite I, Sacramento CA
510(k) summary
Summary
Third party review
No

Clearances, product code INI

Trailing 12 months
24 clearances under product code INI in the twelve months to October 2026, January 2026 the highest month at 5.
Show the numbers
Monthly 510(k) clearances under FDA product code INI, trailing twelve months
MonthClearances
November 20251
December 20252
January 20265
February 20262
March 20262
April 20261
May 20261
June 20262
July 20262
August 20262
September 20264
October 20260