# Lifestream Int'L, Inc.

- Location (FDA's records): The Woodlands, TX
- FDA decisions: 23 (1984–1997): 23 510(k) clearances
- Product codes: GEX (7), CAC (2), DTN (1), KKX (1), JDY (1), GEA (1), GDY (1), FTX (1), DTR (1), DXS (1), HMW (1), GBZ (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 3 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Sorin Biomedica, Fiat, USA, Inc.: 1 (https://510kreport.com/company/sorin-biomedica-fiat-usa)
- Scimed: 1 (https://510kreport.com/company/scimed)

## Firms that cite its devices most
- Laserlite, LLC: 1 (https://510kreport.com/company/laserlite)
- Myriad Lase, Inc.: 1 (https://510kreport.com/company/myriad-lase)
- Diomed, Inc.: 1 (https://510kreport.com/company/diomed)

## Its most-cited devices
- K962354: Diomed 15, 30, 60 Surgical Diode Laser (1996), cited by 2
- K914396: Surgi Light Non-Contact Fibers (1991), cited by 1

## Recent decisions
- K964571: Vision Cardioplegia Delivery System (Aug 8, 1997)
- K962354: Diomed 15, 30, 60 Surgical Diode Laser (Sep 11, 1996)
- K920178: Cardiotomy Reservoir W/20 Micron Filiter (May 13, 1993)
- K920618: Autotransfusion Suction Set (Mar 12, 1993)
- K913181: Autologous Blood Processing System (May 20, 1992)
- K914396: Surgi Light Non-Contact Fibers (Dec 23, 1991)
- K912045: TMP Pressure Isolatorr, TMP Pressure Monitor Syst (Oct 31, 1991)
- K911523: Modification to Model 90-1460 Laser Adapter (Apr 22, 1991)

Source page: https://510kreport.com/company/lifestream-int-l