Home › Device types › HBF
Drills, Burrs, Trephines & Accessories (Compound, Powered)
FDA product code HBF · Class 2 · Neurology
194
Registered devices
2,723
Adverse events
6
Recalls
19
510(k) clearances
Devices with this code
EasyDrill Cranial Perforator Ø11 x Ø7 x 3mm — Micromar Indústria e Comércio LtdaDisposable Cranial Perforator — ACRA-CUT INCNA — Anspach Effort, TheNA — Synthes GmbHACRA-CUT — ACRA-CUT INCNA — Anspach Effort, TheNA — Anspach Effort, TheNA — Anspach Effort, TheNA — Anspach Effort, TheMeridian Perforator — adeor Medical AGAcra-Cut Reusable Cranial Perforator — ACRA-CUT INCEvonos — evonos GmbH & Co. KGACRA-CUT — ACRA-CUT INCCODMAN — Cerenovus, Inc.NA — Anspach Effort, TheNA — Anspach Effort, TheEasyDrill Cranial Perforator Ø14 x Ø11 x 3mm — Micromar Indústria e Comércio LtdaNA — Anspach Effort, TheNA — Anspach Effort, TheNA — Anspach Effort, TheNA — Anspach Effort, TheNA — Anspach Effort, TheACRA-CUT — ACRA-CUT INCNA — Anspach Effort, The
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-09-26 | Integra LifeSciences Corp. (NeuroSciences) | Expansion of recall of size 14 mm Codman Disposable Perforators for inadequate welds to size 11 mm and 9 mm Codman Disposable Perforators out of an abundance of |
| 2025-09-26 | Integra LifeSciences Corp. (NeuroSciences) | Expansion of recall of size 14 mm Codman Disposable Perforators for inadequate welds to size 11 mm and 9 mm Codman Disposable Perforators out of an abundance of |
| 2025-04-11 | Integra LifeSciences Corp. (NeuroSciences) | Inadequate weld that can potentially cause the product to disassemble. |
| 2025-04-11 | Integra LifeSciences Corp. (NeuroSciences) | Inadequate weld that can potentially cause the product to disassemble. |
| 2020-10-16 | Stryker Instruments Div. of Stryker Corporation | Potential for the inner bit to contain a crack, that may or may not be visible, which may lead to metal fragments entering the surgical site and/or delayed dise |
| 2011-07-08 | Biomet Microfixation, Inc. | Biomet Microfixation, Inc., Jacksonville, FL, recalled their IQ Intelligent Device, 72-1000 due to failure of the front bit sensor to detect the correct bit tha |
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 docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.