Home › Device types › FGY
Cannula, Injection
FDA product code FGY · Class 1 · General, Plastic Surgery
86
Registered devices
74
Adverse events
7
Recalls
2
510(k) clearances
Devices with this code
RIN-11-196-CT — RANFAC CORP.ACE — ACE SURGICAL SUPPLY CO., INC.Integra® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONCER-SUB-1111-OT-BNT — RANFAC CORP.Robbins Microcannulas — Robbins Instruments Inc.IV cannula — Tianck Medical Co., Ltd.CER-SUB-1560 — RANFAC CORP.ACE — ACE SURGICAL SUPPLY CO., INC.RIN-11-120-CT — RANFAC CORP.Millennium — Avalign Technologies, Inc.TwoVu — Cannuflow, Inc.IV cannula — Tianck Medical Co., Ltd.Vacuette — Greiner Bio-One GmbHACE — ACE SURGICAL SUPPLY CO., INC.ACE — ACE SURGICAL SUPPLY CO., INC.AccuPort Multi Cannulated 8 GA x 200mm — Zimmer Knee Creations, Inc.RIN-11-11, Component Two — RANFAC CORP.ACE — ACE SURGICAL SUPPLY CO., INC.AccuPort Zone Delivery 8 Ga x 150mm Drill Length — Zimmer Knee Creations, Inc.IV cannula — Tianck Medical Co., Ltd.Ceros — Rhino Medical Supply IncACE — ACE SURGICAL SUPPLY CO., INC.ACE — ACE SURGICAL SUPPLY CO., INC.CER-SUB-825-M — RANFAC CORP.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2022-07-29 | Hobbs Medical, Inc. | Device label display an incorrect expiration date, extends the shelf life of the product. Affected product distributed in the United States from 3/25/2018 to 9 |
| 2015-01-23 | Biologic Therapies, Inc | Devices are misbranded - failure to properly classify and obtain FDA clearance prior distribution |
| 2015-01-23 | Biologic Therapies, Inc | Devices are misbranded - failure to properly classify and obtain FDA clearance prior distribution |
| 2015-01-23 | Biologic Therapies, Inc | Devices are misbranded - failure to properly classify and obtain FDA clearance prior distribution |
| 2013-11-26 | Becton Dickinson & Company | BD Interlink Threaded Lock Cannula REF# 303369 and lot #3021392 is being recalled due to the potential that a small percentage of the lot may exhibit open seals |
| 2013-05-14 | Maquet Cardiovascular Us Sales, Llc | The specified part numbers and lot numbers of Maquet Pediatric Arterial Cannula Packs may contain an incorrectly sized connector. |
| 2005-10-31 | Wilson-Cook Medical Inc | Misbranded; The catheter size listed on the product label is 6 French, which is inaccurate. The catheter size is more accurately described as 7 French. |
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