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"NitraGrip 12"" Pair"

Model MGSE5124 · Medgluv Inc. · DI 00898110000337

LZAPolymer Patient Examination Glove · Class I · 21 CFR 880.6250

LZCMedical Glove, Specialty · Class I · 21 CFR 880.6250

UDILibrary device dossier · generated 2026-09-14 · 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.

23562019-03: 0 reports for this device; peer average 1.2/device2019-05: 0 reports for this device; peer average 3/device2019-08: 0 reports for this device; peer average 1/device2019-11: 0 reports for this device; peer average 1/device2020-09: 0 reports for this device; peer average 1/device2020-12: 0 reports for this device; peer average 1/device2021-02: 0 reports for this device; peer average 1/device2021-03: 0 reports for this device; peer average 1/device2021-05: 0 reports for this device; peer average 2/device2021-08: 0 reports for this device; peer average 1/device2022-02: 0 reports for this device; peer average 1/device2022-03: 0 reports for this device; peer average 1/device2022-04: 0 reports for this device; peer average 1/device2022-09: 0 reports for this device; peer average 1/device2022-11: 0 reports for this device; peer average 1/device2023-02: 0 reports for this device; peer average 1/device2023-04: 0 reports for this device; peer average 1/device2023-12: 0 reports for this device; peer average 1.75/device2024-01: 0 reports for this device; peer average 3/device2024-03: 0 reports for this device; peer average 1/device2024-04: 0 reports for this device; peer average 1/device2024-05: 0 reports for this device; peer average 1.4/device2024-06: 0 reports for this device; peer average 1/device2024-07: 0 reports for this device; peer average 1.5/device2024-08: 0 reports for this device; peer average 2/device2024-09: 0 reports for this device; peer average 1/device2024-10: 0 reports for this device; peer average 2/device2024-11: 0 reports for this device; peer average 1/device2024-12: 0 reports for this device; peer average 3.17/device2025-03: 0 reports for this device; peer average 2/device2025-04: 0 reports for this device; peer average 2/device2025-07: 0 reports for this device; peer average 3/device2025-08: 0 reports for this device; peer average 2/device2025-09: 0 reports for this device; peer average 2/device2025-10: 0 reports for this device; peer average 2/device2025-11: 0 reports for this device; peer average 1/device2025-12: 0 reports for this device; peer average 2/device2026-01: 0 reports for this device; peer average 2.5/device2026-02: 0 reports for this device; peer average 4/device2026-03: 0 reports for this device; peer average 2/device2026-04: 0 reports for this device; peer average 6.38/device2026-05: 0 reports for this device; peer average 5.42/device2026-06: 0 reports for this device; peer average 3/device03050811091202030508020304091102041201030405060708091011120304070809101112010203040506
Monthly adverse-event reports for this device versus the product-code average.
MonthThis device (reports)Product-code average (reports per device)
2019-0301.2
2019-0503
2019-0801
2019-1101
2020-0901
2020-1201
2021-0201
2021-0301
2021-0502
2021-0801
2022-0201
2022-0301
2022-0401
2022-0901
2022-1101
2023-0201
2023-0401
2023-1201.75
2024-0103
2024-0301
2024-0401
2024-0501.4
2024-0601
2024-0701.5
2024-0802
2024-0901
2024-1002
2024-1101
2024-1203.17
2025-0302
2025-0402
2025-0703
2025-0802
2025-0902
2025-1002
2025-1101
2025-1202
2026-0102.5
2026-0204
2026-0302
2026-0406.38
2026-0505.42
2026-0603
This device (reports/month)Average device in LZA, LZC (reports/device/month)

Regulatory clearances

  • None linked in the loaded window.

Manufacturer compliance record — Medgluv Inc.

Nothing in the loaded window.