# K103549: Denovo Teddy Gel Infant Heel Warmer

- Pathway: 510(k) (Traditional)
- Applicant: Denovo Products, LLC
- Decided: Apr 8, 2011 after 126 days
- Product code: MPO (Infant Heel Warmer (Chemical Heat Pack))
- Device class: 1
- Regulation: 21 CFR 890.5710
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
For use by hospital, Ambulatory Surgery staff, Outpatient Clinics for warming of Infant’s Heels prior to drawing blood for sampling or general analysis. This device is intended for Rx use only. This device is single use, non-sterile, and disposable.

Source page: https://510kreport.com/device/K103549
Methodology: https://510kreport.com/methodology