FDA Device Intelligence
Home › LTS Therapy Systems, LLC › Travanti

Travanti

LTS Therapy Systems, LLC · Model SP · UDI-DI 20815611021023

1
510(k) clearances
0
Adverse events
0
Recalls
0
Facilities

Description

This kit contains two (2) devices: 1) IontoPatch: Primary DI Number, 10815611020029 2) Saline: Primary DI Number, 04026704396047 The IontoPatch is single use and disposable. The patch is used in conjunction with the saline.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.