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AED

Model 22-2730 · NATIONAL ADVANCED ENDOSCOPY DEVICES, INC. · DI 00848657006521

KBD — Scissors, Nasal · Class I · 21 CFR 874.4420

UDILibrary device dossier · generated 2026-09-11 · sources: FDA GUDID, openFDA (recalls, MAUDE, 510(k)/PMA), FDA Data Dashboard (inspections, compliance actions), 510(k) summary documents.

Recall history (0)

No recalls linked in the loaded window.

Adverse-event reports — MAUDE (0)

Caveat (required reading): MAUDE report counts cannot be used to compute incidence rates or compare device safety. Reporting is incomplete, duplicated, and spikes with publicity; there is no denominator of devices in use. The peer line is a reporting baseline (average device in the same product code), not a risk measure.

Monthly adverse-event reports for this device versus the product-code average.
Month	This device (reports)	Product-code average (reports per device)
2023-12	0	1
2024-08	0	3
2025-06	0	2
2026-03	0	1

This device (reports/month)Average device in KBD (reports/device/month)

Regulatory clearances

None linked in the loaded window.

Manufacturer compliance record — NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.

VAI 2024-01-12 National Advanced Endoscopy Devices Inc · 0 citations
VAI 2024-01-12 National Advanced Endoscopy Devices Inc · 0 citations
VAI 2020-09-03 National Advanced Endoscopy Devices Inc · 1 citations
VAI 2020-09-03 National Advanced Endoscopy Devices Inc · 1 citations
VAI 2019-08-30 National Advanced Endoscopy Devices Inc · 1 citations
VAI 2019-08-30 National Advanced Endoscopy Devices Inc · 1 citations
VAI 2015-10-26 National Advanced Endoscopy Devices Inc · 3 citations
VAI 2015-10-26 National Advanced Endoscopy Devices Inc · 3 citations
NAI 2012-07-17 National Advanced Endoscopy Devices Inc · 0 citations
NAI 2012-07-17 National Advanced Endoscopy Devices Inc · 0 citations