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EZ-Chek

REPROCESSING PRODUCTS CORPORATION · Model K100-0104 · UDI-DI 00858293006151

MNV Prescription
1
510(k) clearances
0
Adverse events
1
Recalls
2
Facilities

Description

0 -14 pH Test Strips

Recalls

DateFirmReason
2003-02-25Deroyal Surgical -Rose HillNon-sterile surgical medical device is labeled as sterile product.

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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.