Bailey Mfg. Co.: FDA filings under this applicant name
FDA lists 11 510(k) clearances under the applicant name “Bailey Mfg. Co.” (first 1993, latest 1994), across 3 product codes in 1 review panel. Median 510(k) review time under this name: 76 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 |
|---|---|---|---|
| INQ | Table, Powered | 6 | 6 |
| INW | Table, Mechanical | 4 | 4 |
| IRR | Bars, Parallel, Powered | 1 | 1 |
Review panels
- Physical Medicine (11)
Most recent Bailey Mfg. Co. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K932240 | MODEL 5200-10,5200-12 HI-LOW ELEC. PARRALLEL BARS | IRR | 1994-04-01 | 329 |
| K932241 | ECONOMY HI-LOW MAT TABLES/ELECTRIC MODELS | INQ | 1993-07-22 | 76 |
| K932239 | ELECTRIC TILT TABLE MODEL 9505 | INQ | 1993-07-22 | 76 |
| K932238 | ECO. HI-LOW TREATMENT TABLES VARIOUS MODEL NUMBERS | INW | 1993-07-22 | 76 |
| K932237 | PRO. HI-LOW TREATMENT TABLES MODELS 4050,4070,4090 | INQ | 1993-07-22 | 76 |
| K932236 | PRO. HI-LOW TABLE MODEL 9530 | INQ | 1993-07-22 | 76 |
| K932235 | PRO. HI-LOW MAT TABLES #9610-9612 9620-9622 | INQ | 1993-07-22 | 76 |
| K932234 | PROFESSIONAL & ECONMY TILT TABLE 9500 9520 | INW | 1993-07-22 | 76 |
| K932233 | ECONOMY HI-LOW WORK TABLE (MANUAL) MODEL 3405 | INW | 1993-07-22 | 76 |
| K932232 | PROFESSONAL HI-LOW WORK TABLE MODEL 3400 | INQ | 1993-07-22 | 76 |
1 earlier clearances. See the full list in Caduvo.
Recalls
openFDA lists no recalls under a recalling firm named Bailey Mfg. Co..
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.
Other FDA applicant names starting with the same word
FDA records these as separate applicants. Some may belong to the same corporate group and some may not; their filings are not included in the counts above.
- Bailey Medical Engineering (2 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Bailey Mfg. Co.?
FDA lists 11 510(k) clearances under the applicant name “Bailey Mfg. Co.” (first 1993, latest 1994), across 3 product codes 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 Bailey Mfg. Co.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Bailey Mfg. Co. is 76 days.
Which FDA product codes appear under Bailey Mfg. Co.?
The most frequent FDA product codes under this applicant name are INQ (Table, Powered, 6); INW (Table, Mechanical, 4); IRR (Bars, Parallel, Powered, 1).
Next steps
- See all 11 Bailey Mfg. Co. clearances with predicates and recalls
- Run predicate analysis for product code INQ, Bailey Mfg. Co.'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, with punctuation and legal suffixes removed; filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.