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Acra Clip
Model 500-112 · ACRA-CUT INC · DI 00810607000217
HBO — Clip, Scalp · Class II · 21 CFR 882.4150
UDILibrary device dossier · generated 2026-09-07 · 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.
| Month | This device (reports) | Product-code average (reports per device) |
|---|---|---|
| 2019-01 | 0 | 2 |
| 2019-10 | 0 | 22 |
| 2021-04 | 0 | 2 |
| 2021-07 | 0 | 1 |
| 2021-09 | 0 | 1 |
| 2022-03 | 0 | 1 |
| 2022-09 | 0 | 1 |
| 2023-07 | 0 | 1 |
| 2023-12 | 0 | 5 |
| 2024-02 | 0 | 2 |
| 2025-02 | 0 | 1 |
| 2025-05 | 0 | 2 |
Regulatory clearances
- None linked in the loaded window.
Manufacturer compliance record — ACRA-CUT INC
- VAI 2017-10-16 Acra Cut, Inc. · 3 citations
- VAI 2017-10-16 Acra Cut, Inc. · 3 citations
- VAI 2012-12-14 Acra Cut, Inc. · 1 citations
- VAI 2012-12-14 Acra Cut, Inc. · 1 citations
- VAI 2010-10-22 Acra Cut, Inc. · 1 citations
- VAI 2010-10-22 Acra Cut, Inc. · 1 citations