How many FDA warning letters has Technological Medical Advancements LLC received?

Argus HQ has not recorded an FDA warning letter for Technological Medical Advancements LLC in our current dataset.

What FDA recalls has Technological Medical Advancements LLC issued?

Argus HQ has recorded 1 FDA recall tied to Technological Medical Advancements LLC.

Is Technological Medical Advancements LLC FDA compliant?

Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 1 recall, and 0 approval records for Technological Medical Advancements LLC. Review the linked FDA source records directly before drawing a compliance conclusion.

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company

Technological Medical Advancements LLC

Name: FDA Enforcement Actions Against Technological Medical Advancements LLC
Creator: Argus HQ
License: https://argushq.ai/methodology

Jurisdiction: US

FDA Warning Letter timeline

V1 scope: FDA Warning Letters only. Additional public-record sources (SEC, CPSC, federal contracts) are on the V2 roadmap and are not surfaced here today.

fda_recall · device_recall2026-05-20
Technological Medical Advancements LLC — Class II recall: Diowave Laser System, REF: Diowave 250W

Frequently asked questions

How many FDA warning letters has Technological Medical Advancements LLC received?: Argus HQ has not recorded an FDA warning letter for Technological Medical Advancements LLC in our current dataset.
What FDA recalls has Technological Medical Advancements LLC issued?: Argus HQ has recorded 1 FDA recall tied to Technological Medical Advancements LLC.
Is Technological Medical Advancements LLC FDA compliant?: Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 1 recall, and 0 approval records for Technological Medical Advancements LLC. Review the linked FDA source records directly before drawing a compliance conclusion.

Informational only. FDA Warning Letters are public records (17 USC §105). Summaries are AI-assisted and may contain errors; always verify against the original FDA letter before acting. Not legal, financial, or regulatory advice.