Thomas Industries: FDA filings under this applicant name
FDA lists 9 510(k) clearances under the applicant name “Thomas Industries” (first 1994, latest 2004), across 3 product codes in 2 review panels. Median 510(k) review time under this name: 129 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 |
|---|---|---|---|
| BTA | Pump, Portable, Aspiration (Manual Or Powered) | 5 | 5 |
| BTI | Compressor, Air, Portable | 2 | 2 |
| CAF | Nebulizer (Direct Patient Interface) | 2 | 2 |
Review panels
Most recent Thomas Industries 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K041199 | MEDI-PUMP ASPIRATOR, MODEL 1615 | BTA | 2004-06-01 | 25 |
| K965059 | CPI, MAXI-VAC(6480),THOMAS INDUSTRIES, MEDI-PUMP(1240/1242/1243) | BTA | 1997-03-04 | 76 |
| K952806 | MEDI PUMP ASPIRATOR MODELS 1130 AND 1135 | BTA | 1995-10-26 | 129 |
| K950290 | MEDI - PUMP | CAF | 1995-08-24 | 211 |
| K951729 | MEDI - PUMP | BTA | 1995-08-21 | 129 |
| K950867 | MEDI - PUMP | CAF | 1995-04-19 | 51 |
| K944399 | MEDI-PUMP | BTA | 1995-01-18 | 132 |
| K925010 | NEBULIZER PUMP, POWERED, MODEL 1110 | BTI | 1994-05-27 | 602 |
| K925011 | NEBULIZER PUMP, POWERED MODEL 1180 | BTI | 1994-01-12 | 467 |
Recalls
openFDA lists no recalls under a recalling firm named Thomas Industries.
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.
Related HCPCS codes
HCPCS Level II codes whose descriptors match the device names of the product codes filed under Thomas Industries (a text match, not an official crosswalk):
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.
- Thomas Medical Products, Inc. (23 510(k)s)
- Thomas J. Fogarty, M.D. (6 510(k)s)
- Thomas Medical, Inc. (2 510(k)s)
- Thomas G. Mason (1 510(k)s)
- Thomas M. Foti, M.D. (1 510(k)s)
- Thomas Surgical Instruments, Inc. (1 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Thomas Industries?
FDA lists 9 510(k) clearances under the applicant name “Thomas Industries” (first 1994, latest 2004), across 3 product codes in 2 review panels. Filings under other applicant names, such as subsidiaries, are not included.
How long has FDA taken to clear 510(k)s filed by Thomas Industries?
The median time from FDA receipt to decision across 510(k)s cleared under the name Thomas Industries is 129 days.
Which FDA product codes appear under Thomas Industries?
The most frequent FDA product codes under this applicant name are BTA (Pump, Portable, Aspiration (Manual Or Powered), 5); BTI (Compressor, Air, Portable, 2); CAF (Nebulizer (Direct Patient Interface), 2).
Next steps
- See all 9 Thomas Industries clearances with predicates and recalls
- Run predicate analysis for product code BTA, Thomas Industries'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.