Tri W-G, Inc.: FDA filings under this applicant name
FDA lists 35 510(k) clearances under the applicant name “Tri W-G, Inc.” (first 1979, latest 1996), across 15 product codes in 4 review panels. Median 510(k) review time under this name: 36 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 | 14 | 14 |
| IXR | Table, Radiographic, Tilting | 3 | 3 |
| BXB | Exerciser, Powered | 2 | 2 |
| IMC | Bath, Paraffin | 2 | 2 |
| ISD | Exerciser, Measuring | 2 | 2 |
| JFB | Table, Physical Therapy, Multi Function | 2 | 2 |
| GZJ | Stimulator, Nerve, Transcutaneous, For Pain Relief | 1 | 1 |
| IKZ | Bed, Patient Rotation, Powered | 1 | 1 |
| INK | Stretcher, Wheeled, Powered | 1 | 1 |
| INW | Table, Mechanical | 1 | 1 |
Plus 5 more product codes.
Review panels
- Physical Medicine (28)
- Radiology (3)
- General Hospital (1)
- Neurology (1)
Most recent Tri W-G, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K960196 | TRI W-G, INC TABLE, TILT/EXAM/TREATMENT MODEL 777 | INQ | 1996-02-07 | 22 |
| K945163 | ECHOCARDIOGRAPHY | LGX | 1995-02-17 | 119 |
| K941720 | MODEL 747 AND 747-30 EXAM/TREATMENT TABLE | INQ | 1994-05-06 | 29 |
| K936303 | TREATMENT TABLE MODIFICATION | INQ | 1994-03-18 | 119 |
| K933119 | HI-LO TREATMENT TABLES | INQ | 1993-10-12 | 109 |
| K932746 | MODEL T4501,T4502,T4503,T4504,T4504 TILT TABLE | INQ | 1993-07-21 | 43 |
| K930802 | MODELS 642 & 643 TILT EXAM/TREATMENT TABLE | INQ | 1993-03-22 | 34 |
| K925594 | MDL 29001 MEDI ELEC-MECH TILT EXAM/TREATMENT TABLE | INQ | 1993-02-12 | 99 |
| K923325 | MODEL 600 MEDICAL TREATMENT TABLE | INQ | 1992-07-21 | 14 |
| K922980 | 745-M (MAGNUM) | JFB | 1992-07-13 | 21 |
25 earlier clearances. See the full list in Caduvo.
Recalls
openFDA lists no recalls under a recalling firm named Tri W-G, 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 Tri W-G, Inc.?
FDA lists 35 510(k) clearances under the applicant name “Tri W-G, Inc.” (first 1979, latest 1996), across 15 product codes in 4 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 Tri W-G, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Tri W-G, Inc. is 36 days.
Which FDA product codes appear under Tri W-G, Inc.?
The most frequent FDA product codes under this applicant name are INQ (Table, Powered, 14); IXR (Table, Radiographic, Tilting, 3); BXB (Exerciser, Powered, 2).
Next steps
- See all 35 Tri W-G, Inc. clearances with predicates and recalls
- Run predicate analysis for product code INQ, Tri W-G, 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.