FDA product code LSA: Vise, Bench, Surgical
LSA is the FDA product code for vise, bench, surgical. It is a Class I device, regulated under 21 CFR 878.4800 and reviewed by the General and Plastic Surgery panel. FDA has cleared 1 510(k) submission under LSA. The average 510(k) review took 27 days (median 27).
Classification
| Field | Value |
|---|---|
| Device name | Vise, Bench, Surgical |
| Device class | Class I |
| Regulation | 21 CFR 878.4800 |
| Review panel | SU — General and Plastic Surgery |
| Medical specialty | General, Plastic Surgery |
| Premarket route | 510(k) exempt |
Compare with all 510(k) review times · Search every LSA clearance
Top LSA applicants
| Applicant | Clearances | Latest |
|---|---|---|
| Med-Tool, Inc. | 1 | 1987-07-16 |
Most recent LSA clearances
| 510(k) | Applicant | Device | Decision date | Review days |
|---|---|---|---|---|
| K872385 | Med-Tool, Inc. | VICE OR BENCH VICE | 1987-07-16 | 27 |
Recalls for LSA devices
openFDA lists no recalls for product code LSA.
Frequently asked questions
What is FDA product code LSA?
LSA is the FDA product code for vise, bench, surgical. It is a Class I device, regulated under 21 CFR 878.4800 and reviewed by the General and Plastic Surgery panel.
What device class is LSA?
Class I, regulation 21 CFR 878.4800. Typical premarket route: 510(k) exempt.
How long does a 510(k) take for product code LSA?
Across 1 cleared submissions the average was 27 days from receipt to decision (median 27).
Which companies have the most LSA clearances?
Med-Tool, Inc. (1).
Next steps
- Run an FDA pathway report with predicate devices for product code LSA
- Run a recall and safety report across every LSA manufacturer
- Watch product code LSA for new clearances and recalls
Source: openFDA device classification, 510(k), PMA, De Novo and recall data (public domain). Review days run from FDA receipt to decision. Not regulatory advice.
All General and Plastic Surgery product codes · FDA product code lookup · 510(k) database search · 510(k) review times