MallyaD injection pen adapter (MallyaD)

FDA 510(k) K250555 · Biocorp Production

Substantially Equivalent

510(k) numberK250555

Submission

Device name
MallyaD injection pen adapter (MallyaD)
Applicant
Biocorp Production
Issoire, FR
Received
February 25, 2025
Decision date
March 27, 2025
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
QOG – Injection Data Capture Device
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5860
Specialty
General Hospital

An injection data capture device is an electrically-powered/electromechanical accessory that interfaces with reusable or disposable injection devices for the purposes of interpreting, recording and displaying and/or transmitting injection data to a connected application or software.

Other 510(k)s with product code QOG

510(k)DeviceApplicantDecision
K243901SmartPilot YpsoMate NS-A2.25QOG · Traditional Ypsomed AG08/28/2025SE
K251500MallyaG Injection Pen Adapter (MallyaG)QOG · Special Biocorp Production06/09/2025SE
K241803INSULCLOCK® v2.0 PROQOG · Traditional Insulcloud S.L.08/22/2024SE
K231820SoloSmart Injection Pen Adapter (SoloSmart®)QOG · Special Biocorp Production01/12/2024SE
K222689Mallya Injection Pen Adapter (Mallya® for Solostar®)QOG · Traditional Biocorp Production12/05/2022SE
K212217Tempo Smart ButtonQOG · Traditional Eli Lilly and Company09/16/2022SE

More from Eli Lilly and Company

510(k)DeviceDecision
K251500MallyaG Injection Pen Adapter (MallyaG)QOG · Special 06/09/2025SE
K231820SoloSmart Injection Pen Adapter (SoloSmart®)QOG · Special 01/12/2024SE
K222689Mallya Injection Pen Adapter (Mallya® for Solostar®)QOG · Traditional 12/05/2022SE

Questions and answers

When was MallyaD injection pen adapter (MallyaD) cleared by the FDA?

MallyaD injection pen adapter (MallyaD) (K250555) received a 510(k) decision of Substantially Equivalent on March 27, 2025, 30 days after the submission was received.

What is the product code of K250555?

The FDA product code is QOG – Injection Data Capture Device, a Class II (moderate risk) device regulated under 21 CFR 880.5860.