FDA applicant
Life-Tech, Inc.
FDA records 14 decisions for Life-Tech, Inc. (Stafford, TX) from 2005 to 2012: 14 510(k) clearances. Most are in product codes CAZ (Anesthesia Conduction Kit) and BSP (Needle, Conduction, Anesthetic (W/Wo Introducer)). No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Life-Tech, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2012
2007high 4 (2008) · low 0 (2013)2026
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Life-Tech, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report