Slenderizers Equipment Mfg., Inc.: FDA filings under this applicant name
FDA lists 7 510(k) clearances under the applicant name “Slenderizers Equipment Mfg., Inc.” (first 1987, latest 1988), across 1 product code in 1 review panel. Median 510(k) review time under this name: 109 days. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.
510(k) clearances per year
| Year | Clearances | Median review days |
|---|---|---|
| 2012 | 0 | — |
| 2013 | 0 | — |
| 2014 | 0 | — |
| 2015 | 0 | — |
| 2016 | 0 | — |
| 2017 | 0 | — |
| 2018 | 0 | — |
| 2019 | 0 | — |
| 2020 | 0 | — |
| 2021 | 0 | — |
| 2022 | 0 | — |
| 2023 | 0 | — |
| 2024 | 0 | — |
| 2025 | 0 | — |
| 2026 | 0 | — |
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| JFB | Table, Physical Therapy, Multi Function | 7 | 7 |
Review panels
Most recent Slenderizers Equipment Mfg., Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K881804 | MULTI-FLEX TABLE--MODEL 200 | JFB | 1988-07-15 | 78 |
| K870715 | MULTI-FLEX TABLE -- MODEL 106 | JFB | 1987-06-09 | 109 |
| K870714 | MULTI-FLEX TABLE -- MODEL 105 | JFB | 1987-06-09 | 109 |
| K870713 | MULTI-FLEX TABLE -- MODEL 104 | JFB | 1987-06-09 | 109 |
| K870712 | MULTI-FLEX TABLE -- MODEL 103 | JFB | 1987-06-09 | 109 |
| K870711 | MULTI-FLEX TABLE -- MODEL 102 | JFB | 1987-06-09 | 109 |
| K870710 | MULTI-FLEX TABLE -- MODEL 101 | JFB | 1987-06-09 | 109 |
Recalls
openFDA lists no recalls under a recalling firm named Slenderizers Equipment Mfg., Inc..
Recalling firms are matched to this applicant name by name only (same normalization), so related entities that recall under another name are not counted. A recall count says nothing about how safe one company's devices are compared with another's.
Frequently asked questions
How many FDA 510(k) clearances are listed under Slenderizers Equipment Mfg., Inc.?
FDA lists 7 510(k) clearances under the applicant name “Slenderizers Equipment Mfg., Inc.” (first 1987, latest 1988), across 1 product code in 1 review panel. Filings under other applicant names, such as subsidiaries, are not included.
How long has FDA taken to clear 510(k)s filed by Slenderizers Equipment Mfg., Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Slenderizers Equipment Mfg., Inc. is 109 days.
Which FDA product codes appear under Slenderizers Equipment Mfg., Inc.?
The most frequent FDA product codes under this applicant name are JFB (Table, Physical Therapy, Multi Function, 7).
Next steps
- See all 7 Slenderizers Equipment Mfg., Inc. clearances with predicates and recalls
- Run predicate analysis for product code JFB, Slenderizers Equipment Mfg., Inc.'s most frequent
Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Each page covers one FDA applicant name (spelling variants such as punctuation and legal suffixes combined); filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.