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DMI

D-M-S HOLDINGS, INC. · Model 650-2600-0020 · UDI-DI 00041298992370

OHO
0
510(k) clearances
5
Adverse events
1
Recalls
235
Facilities

Description

First Aid Kit - 20pcs

Recalls

DateFirmReason
2026-07-07INTEGRATED MEDCRAFT LLCDevices could potentially contain an occluded or partially occluded Guedel Airway tip.

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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.