Home › Device types › HXY
Brace, Drill
FDA product code HXY · Class 1 · Orthopedic
160
Registered devices
44
Adverse events
1
Recalls
7
510(k) clearances
Devices with this code
Spider Cervical Plating System — Xtant Medical Holdings, Inc.BR Surgical, LLC — BR Surgical, LLCNovo Surgical Inc. — NOVO SURGICAL, INC.Medicon — Medicon eG. Chirurgiemechaniker-GenossenschaftMedicon — Medicon eG. Chirurgiemechaniker-GenossenschaftVolition Plating System — ORTHO SOLUTIONS HOLDINGS LIMITEDMedicon — Medicon eG. Chirurgiemechaniker-GenossenschaftACCULAN II — Aesculap AGMedicon — Medicon eG. Chirurgiemechaniker-GenossenschaftCitrelock ACL Tibial Drill Guide — Acuitive Technologies, Inc.AESCULAP — Aesculap AGLINK Embrace Shoulder System Line Extension — WALDEMAR LINK GmbH & Co. KGOrthoSolutions 'System26' Bone Screws — ORTHO SOLUTIONS HOLDINGS LIMITEDAESCULAP — Aesculap AGOrthoSolutions 'System26' Bone Screws — ORTHO SOLUTIONS HOLDINGS LIMITEDAESCULAP — Aesculap AGMedicon — Medicon eG. Chirurgiemechaniker-GenossenschaftKMEDIC — TELEFLEX INCORPORATEDMedicon — Medicon eG. Chirurgiemechaniker-GenossenschaftAnchor Pin — CAPTIVA SPINE, INC.Medicon — Medicon eG. Chirurgiemechaniker-GenossenschaftTransFasten - LSF, Open-Ended Offset Guide — CAPTIVA SPINE, INC.Spider Cervical Plating System — Xtant Medical Holdings, Inc.BIOPSYBELL — BIOPSYBELL SRL
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2015-05-27 | Musculoskeletal Transplant Foundation, Inc. | Musculoskeletal Transplant Foundation is recalling a certain lot of Allofix Insertion Kits because they are labeled as having a 2.0mm diameter drill however it |
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.