FDA applicant

Lifemed Technologies, Inc.

Houston, TX1 decision1986–19860 recalls

FDA records 1 decision for Lifemed Technologies, Inc. (Houston, TX) in 1986: 1 510(k) clearance. All are in product code KZD (Infusor, Pressure, For I.V. Bags). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general hospital panel, where it files most

How often FDA has decided Lifemed Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Lifemed Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Lifemed Technologies, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Lifemed Technologies, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Lifemed”

FDA records each applicant name separately; these may or may not be the same firm.

Lifemed of California 4

Lifemed Technologies, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Lifemed”