FDA Device Intelligence
HomeDevice types › HBC

Motor, Drill, Electric

FDA product code HBC · Class 2 · Neurology

1,727
Registered devices
28,221
Adverse events
39
Recalls
26
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2022-12-07The Anspach Effort, Inc.Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome Attachment) came out of the attachment, possibly during removal of the attachment, intra-oper
2022-12-07The Anspach Effort, Inc.Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome Attachment) came out of the attachment, possibly during removal of the attachment, intra-oper
2022-12-07The Anspach Effort, Inc.Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome Attachment) came out of the attachment, possibly during removal of the attachment, intra-oper
2022-12-07The Anspach Effort, Inc.Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome Attachment) came out of the attachment, possibly during removal of the attachment, intra-oper
2022-12-07The Anspach Effort, Inc.Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome Attachment) came out of the attachment, possibly during removal of the attachment, intra-oper
2022-12-07The Anspach Effort, Inc.Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome Attachment) came out of the attachment, possibly during removal of the attachment, intra-oper
2022-12-07The Anspach Effort, Inc.Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome Attachment) came out of the attachment, possibly during removal of the attachment, intra-oper
2022-12-07The Anspach Effort, Inc.Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome Attachment) came out of the attachment, possibly during removal of the attachment, intra-oper
2022-12-07The Anspach Effort, Inc.Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome Attachment) came out of the attachment, possibly during removal of the attachment, intra-oper
2016-10-06The Anspach Effort, Inc.Supplied Directions for Use (DFU) did not contain a recommended service interval.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.