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Litetouch

Asp Global, LLC · Model 203TC · UDI-DI 00840216124332

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510(k) clearances

Adverse events

Recalls

Facilities

Description

LITE TOUCH MICRO THIN LANCETS - 33G - 1/EA, 100EA/BX, 100BX/CS (10000EA)

Query this across every FDA database — by API.

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

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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.