LFLUnclassified
Instrument, Ultrasonic Surgical
Unknown
LFL is the FDA product code for Instrument, Ultrasonic Surgical. As of , FDA records hold 158 510(k) clearances under this code, the most recent dated , and 109 recalls.
Classification record
- Product code
- LFL
- Device name
- Instrument, Ultrasonic Surgical
- Device class
- Unclassified
- Review panel
- Unknown
- Submission type
- 510(k)
- Implant
- No
- Life sustaining or supporting
- No
- GMP exempt
- No
- Third party review eligible
- No
- Ingested clearances
- 158
- Ingested recalls
- 109
Clearances, product code LFL
By decision yearShow the numbers
| Year | Clearances |
|---|---|
| 1980 | 1 |
| 1982 | 1 |
| 1983 | 1 |
| 1985 | 2 |
| 1987 | 1 |
| 1988 | 4 |
| 1989 | 1 |
| 1990 | 4 |
| 1991 | 1 |
| 1992 | 1 |
| 1993 | 3 |
| 1994 | 2 |
| 1995 | 2 |
| 1996 | 4 |
| 1997 | 9 |
| 1998 | 9 |
| 1999 | 6 |
| 2000 | 4 |
| 2001 | 7 |
| 2002 | 3 |
| 2003 | 7 |
| 2004 | 3 |
| 2005 | 5 |
| 2006 | 4 |
| 2007 | 7 |
| 2008 | 2 |
| 2009 | 1 |
| 2010 | 2 |
| 2011 | 3 |
| 2012 | 3 |
| 2013 | 5 |
| 2014 | 3 |
| 2015 | 4 |
| 2016 | 5 |
| 2017 | 2 |
| 2018 | 3 |
| 2019 | 4 |
| 2020 | 4 |
| 2021 | 6 |
| 2022 | 8 |
| 2023 | 4 |
| 2024 | 3 |
| 2025 | 3 |
| 2026 | 1 |
Applicants with the most clearances
Product code LFL| Applicant | Clearances |
|---|---|
| Ethicon Endo-Surgery Inc | 29 |
| Integra LifeSciences Corporation | 13 |
| Medtronic, Inc. | 13 |
| Misonix, LLC | 11 |
| Olympus Optical Co., Ltd. | 5 |
| AOMORI OLYMPUS CO., Ltd. Kuroishi Site | 4 |
| Integra Radionics, Inc. | 4 |
| SRA Developments Ltd | 4 |
| Stryker Corp. | 4 |
| Tenex Health | 4 |
Companies listing this code with FDA
Companies whose registered establishments list this codeFIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.