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OnScope(TM) Endoscopic Dilator Kit

Micro-Tech (Nanjing) Co., Ltd. · Model DILA03002 · UDI-DI 06932503525237

KNQ Prescription
10
510(k) clearances
5,261
Adverse events (16 deaths)
21
Recalls
59
Facilities

Description

Dilator Kit(OD=18mm, ID=9.2mm)

Recalls

DateFirmReason
2026-03-18Diversatek HealthcareThe catheter inflation tag attached to the device may contain an incorrect part number with incorrect balloon diameter sizes and inflation pressures for each stage.
2026-03-18Diversatek HealthcareThe catheter inflation tag attached to the device may contain an incorrect part number with incorrect balloon diameter sizes and inflation pressures for each stage.
2026-03-18Diversatek HealthcareThe catheter inflation tag attached to the device may contain an incorrect part number with incorrect balloon diameter sizes and inflation pressures for each stage.
2026-03-18Diversatek HealthcareThe catheter inflation tag attached to the device may contain an incorrect part number with incorrect balloon diameter sizes and inflation pressures for each stage.
2013-05-28Boston Scientific CorporationProduct labeled with incorrect expiration date.
2007-04-16Conmed Endoscopic Technologies, Inc.Mislabeling issues including; incorrect balloon diameters, lot number discrepancies, and incorrect type of dilator.
2007-04-16Conmed Endoscopic Technologies, Inc.Mislabeling issues including; incorrect balloon diameters, lot number discrepancies, and incorrect type of dilator.
2007-04-16Conmed Endoscopic Technologies, Inc.Mislabeling issues including; incorrect balloon diameters, lot number discrepancies, and incorrect type of dilator.
2007-04-16Conmed Endoscopic Technologies, Inc.Mislabeling issues including; incorrect balloon diameters, lot number discrepancies, and incorrect type of dilator.
2007-04-16Conmed Endoscopic Technologies, Inc.Mislabeling issues including; incorrect balloon diameters, lot number discrepancies, and incorrect type of dilator.

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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.