FDA Device Intelligence
Home › PRECEPTIS MEDICAL, INC › Hummingbird Tympanostomy Tube System

Hummingbird Tympanostomy Tube System

PRECEPTIS MEDICAL, INC · Model 05-1001-753 · UDI-DI 00853386007091

ETD Prescription
10
510(k) clearances
92
Adverse events
14
Recalls
36
Facilities

Description

05-1001-753, +90 Inserter With Pre-loaded 1.14mm ID Vent Tube

Recalls

DateFirmReason
2024-11-24Adept Medical LtdLack of 510(k) clearance.
2024-11-24Adept Medical LtdLack of 510(k) clearance.
2024-11-24Adept Medical LtdLack of 510(k) clearance.
2024-11-24Adept Medical LtdLack of 510(k) clearance.
2024-11-24Adept Medical LtdLack of 510(k) clearance.
2024-11-24Adept Medical LtdLack of 510(k) clearance.
2024-11-24Adept Medical LtdLack of 510(k) clearance.
2024-11-24Adept Medical LtdLack of 510(k) clearance.
2024-11-19Olympus Corporation of the AmericasPotential that Duravent Silicone Ventilation Tubes may contain incorrect product, specifically, 1.32 mm Tiny T Tubes (model: 70240076) instead of the intended Duravent Silicone Ven
2023-12-11Olympus Corporation of the AmericasThe expiration date is missing from the primary (inner) packaging. The secondary (outer) box label correctly states the expiration date of February 12, 2033, for this lot

Query this across every FDA database — by API.

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

Get your free API keyRead the docs
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.