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DeRoyal

DEROYAL INDUSTRIES, INC. · Model 89-7548 · UDI-DI 00749756741392

OGS
0
510(k) clearances
0
Adverse events
1
Recalls
13
Facilities

Description

MYRINGOTOMY PACK-LF

Recalls

DateFirmReason
2022-11-17MEDLINE INDUSTRIES, LP - NorthfieldSterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.

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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.