Progressive Medical Technology, Inc.: FDA filings under this applicant name
FDA lists 5 510(k) clearances under the applicant name “Progressive Medical Technology, Inc.” (first 1992, latest 1993), across 3 product codes in 1 review panel. Median 510(k) review time under this name: 56 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 |
|---|---|---|---|
| IRP | Massager, Powered Inflatable Tube | 3 | 3 |
| IKZ | Bed, Patient Rotation, Powered | 1 | 1 |
| IOQ | Bed, Flotation Therapy, Powered | 1 | 1 |
Review panels
Most recent Progressive Medical Technology, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K923710 | OSCILLAIR 3000 LOW AIR LOSS KINETIC THERAPY BED | IKZ | 1993-03-22 | 238 |
| K915638 | TALLEY TM200 INTERMTTENT COMPRESSION UNIT | IRP | 1992-02-11 | 56 |
| K915637 | TALLEY TM500 SEQUENTIAL MULTICOM COMPRESSION SYST. | IRP | 1992-02-11 | 56 |
| K915092 | TALLEY TM300 SEQUENTIAL MULTICOM COMPRESSION SYST | IRP | 1992-02-11 | 82 |
| K915671 | B.A.S.E. BELLOWS AIR SUPPORT EQUIPMENT | IOQ | 1992-01-13 | 49 |
Recalls
openFDA lists no recalls under a recalling firm named Progressive Medical Technology, 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.
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.
- Progressive Electrical Therapeutics (10 510(k)s)
- Progressive Dynamics, Inc. (7 510(k)s)
- Progressive Concepts, Inc. (4 510(k)s)
- Progressive Productions , Ltd. (4 510(k)s)
- Progressive Surgical Products, Inc. (3 510(k)s)
- Progressive Technology, Inc. (3 510(k)s)
- Progressive Affiliated Labs, Inc. (1 510(k)s)
- Progressive Aligners, Inc. (1 510(k)s)
- Progressive Dental Supply (1 510(k)s)
- Progressive Iv'S, Inc. (1 510(k)s)
- Progressive Medical, Inc. (1 510(k)s)
- Progressive Medical Applications Corp. (1 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Progressive Medical Technology, Inc.?
FDA lists 5 510(k) clearances under the applicant name “Progressive Medical Technology, Inc.” (first 1992, latest 1993), 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 Progressive Medical Technology, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Progressive Medical Technology, Inc. is 56 days.
Which FDA product codes appear under Progressive Medical Technology, Inc.?
The most frequent FDA product codes under this applicant name are IRP (Massager, Powered Inflatable Tube, 3); IKZ (Bed, Patient Rotation, Powered, 1); IOQ (Bed, Flotation Therapy, Powered, 1).
Next steps
- See all 5 Progressive Medical Technology, Inc. clearances with predicates and recalls
- Run predicate analysis for product code IRP, Progressive Medical Technology, 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, 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.