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
K103009Substantially Equivalent

Senticare Pillstation

Senticare, Inc., Washington DC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K103009 is the FDA 510(k) clearance record for SENTICARE PILLSTATION, a class I device, cleared for Senticare, Inc. on under FDA product code NXQ (Reminder, Medication). FDA's definition for product code NXQ reads: "A medication reminder is a device intended for medical purposes to provide alerts to patients or healthcare providers for pre-determined medication dosing schedules. The device may incorporate wireless communication". FDA records list one 510(k) clearance for Senticare, Inc. As of , FDA records show no recalls naming K103009.

Clearance record

Decision date
Received
(108 days to decision)
Product code
NXQ Reminder, Medication
Regulation
21 CFR 890.5050
Device class
Class I
Review panel
Physical Medicine
Applicant
Senticare, Inc. 401 9th St. NW, Washington DC
510(k) summary
Summary PDF
Third party review
No

Clearances, product code NXQ

Trailing 12 months

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

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