Midland Mfg. Co.: FDA filings under this applicant name
FDA lists 7 510(k) clearances under the applicant name “Midland Mfg. Co.” (first 1992, latest 1994), across 2 product codes in 1 review panel. Median 510(k) review time under this name: 94 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 |
| BXB | Exerciser, Powered | 1 | 1 |
Review panels
Most recent Midland Mfg. Co. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K933311 | MOTORIZED ELECTRIC PARALLEL BARS | BXB | 1994-01-26 | 203 |
| K925164 | ELECTRIC STAND-IN TABLE | INQ | 1993-03-24 | 162 |
| K924093 | ELECTRIC HI LO TILT TABLE | INQ | 1993-02-12 | 183 |
| K924002 | MIDLAND THREE SECTION P.T. TABLE W/ DRAINAGE | INQ | 1992-11-09 | 91 |
| K923998 | MIDLAND TILT TABLE | INQ | 1992-11-09 | 91 |
| K923973 | SPACE BASE ELECTRIC TILT TABLE | INQ | 1992-11-09 | 94 |
| K924019 | DELUXE ELECTRIC COMBINATION TILT TABLE | INQ | 1992-11-06 | 87 |
Recalls
openFDA lists no recalls under a recalling firm named Midland 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.
Frequently asked questions
How many FDA 510(k) clearances are listed under Midland Mfg. Co.?
FDA lists 7 510(k) clearances under the applicant name “Midland Mfg. Co.” (first 1992, latest 1994), across 2 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 Midland Mfg. Co.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Midland Mfg. Co. is 94 days.
Which FDA product codes appear under Midland Mfg. Co.?
The most frequent FDA product codes under this applicant name are INQ (Table, Powered, 6); BXB (Exerciser, Powered, 1).
Next steps
- See all 7 Midland Mfg. Co. clearances with predicates and recalls
- Run predicate analysis for product code INQ, Midland 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 (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.