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HomeOsteocentric Technologies, Inc. › 4.0mm Drill 110mm

4.0mm Drill 110mm

Osteocentric Technologies, Inc. · Model 321-0003 · UDI-DI 00810074300889

HTW Prescription
1
510(k) clearances
17,754
Adverse events (5 deaths)
114
Recalls
557
Facilities

Description

4.0mm Drill 110mm

Recalls

DateFirmReason
2026-02-11Waldemar Link GmbH & Co. KG (Mfg Site)The surgical technique for the Embrace Shoulder Instruments - Drill Tower has mixed-up article numbers in the overview of the instruments. However, the individual surgical steps de
2026-02-11Waldemar Link GmbH & Co. KG (Mfg Site)The surgical technique for the Embrace Shoulder Instruments - Drill Tower has mixed-up article numbers in the overview of the instruments. However, the individual surgical steps de
2024-01-29Waldemar Link GmbH & Co. KG (Mfg Site)The surgical techniques for the Embrace Shoulder Instruments -Drill Tower (Article REF 645-081/62 & /63) have mixed-up type descriptions ("standard" vs "wedged") in the overview of
2024-01-29Waldemar Link GmbH & Co. KG (Mfg Site)The surgical techniques for the Embrace Shoulder Instruments -Drill Tower (Article REF 645-081/62 & /63) have mixed-up type descriptions ("standard" vs "wedged") in the overview of
2021-09-01Flower Orthopedics CorporationDrill bits packaged in kits are missing the AO connect feature and may result in delay of procedure
2021-09-01Flower Orthopedics CorporationDrill bits packaged in kits are missing the AO connect feature and may result in delay of procedure
2021-09-01Flower Orthopedics CorporationDrill bits packaged in kits are missing the AO connect feature and may result in delay of procedure
2021-09-01Flower Orthopedics CorporationDrill bits packaged in kits are missing the AO connect feature and may result in delay of procedure
2021-07-30Paragon 28, Inc.A thin wall condition between the inner cannulation and the flutes of the drill which potentially could cause a fracture through the wall of the drill to the cannulation beneath.
2021-02-24Arthrex, Inc.The color indicator on the proximal end of the shaft of the AR-8770-02 is the incorrect color.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.