FDA Device Intelligence
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Motor, Surgical Instrument, Pneumatic Powered

FDA product code GET · Class 1 · General, Plastic Surgery

353
Registered devices
1,030
Adverse events
54
Recalls
23
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2023-02-14Pro-Dex IncIncorrect Unique Device Identifier/GTIN code was used on product.
2016-10-06The Anspach Effort, Inc.Supplied Directions for Use (DFU) did not contain a recommended service interval.
2016-10-06The Anspach Effort, Inc.Supplied Directions for Use (DFU) did not contain a recommended service interval.
2016-03-11MicroAire Surgical Instruments, LLCMicroAire discovered that 20 suspect Impactor instruments ( MicroAire Pneumatic Impactor) were shipped to end users and were missing the lock and unlock symbol
2013-12-09Aesculap, Inc.Certain lots of the Aesculap Hi Line XXS handpiece (part # GB790R) were recalled due to a possible failure of the handpiece.
2008-02-21Linvatec Corp.Sterility compromised. There is a possibility that certain catalog number and lots of ConMed Linvatec Hall Surgical Blades, may have a hole(s) in the corner(s)
2008-02-21Linvatec Corp.Sterility compromised. There is a possibility that certain catalog number and lots of ConMed Linvatec Hall Surgical Blades, may have a hole(s) in the corner(s)
2008-02-21Linvatec Corp.Sterility compromised. There is a possibility that certain catalog number and lots of ConMed Linvatec Hall Surgical Blades, may have a hole(s) in the corner(s)
2008-02-21Linvatec Corp.Sterility compromised. There is a possibility that certain catalog number and lots of ConMed Linvatec Hall Surgical Blades, may have a hole(s) in the corner(s)
2008-02-21Linvatec Corp.Sterility compromised. There is a possibility that certain catalog number and lots of ConMed Linvatec Hall Surgical Blades, may have a hole(s) in the corner(s)

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