Innova Corp.: FDA filings under this applicant name
FDA lists 6 510(k) clearances under the applicant name “Innova Corp.” (first 1991, latest 2004), across 3 product codes in 2 review panels. Median 510(k) review time under this name: 47 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 |
|---|---|---|---|
| DZE | Implant, Endosseous, Root-Form | 4 | 4 |
| LYG | Massager, Therapeutic, Manual | 1 | 1 |
| MQN | External Mandibular Fixator And/Or Distractor | 1 | 1 |
Review panels
- Dental (5)
- Physical Medicine (1)
Most recent Innova Corp. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K040714 | HYBRID ENDOPORE ENDOSSEOUS DENTAL IMPLANT | DZE | 2004-04-09 | 22 |
| K984117 | INNOVA TELESCOPIC DISTRACTOR | MQN | 1999-02-10 | 85 |
| K971196 | ENDOPORE ENDOSSEOUS DENTAL IMPLANT SYSTEM | DZE | 1997-05-08 | 38 |
| K952434 | ENDOPORE DENTAL IMPLANT ABUTMENTS | DZE | 1995-07-19 | 56 |
| K926354 | ENDO-PORE ENDOSSEOUS DENTAL IMPLANT SYSTEM | DZE | 1995-02-13 | 784 |
| K915361 | THE BODY BUGGY | LYG | 1991-12-20 | 23 |
Recalls
openFDA lists no recalls under a recalling firm named Innova Corp..
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.
- Innova Vision, Inc. (11 510(k)s)
- Innova Life Sciences Corp. (4 510(k)s)
- Innova Spinal Technologies, LLC (2 510(k)s)
- Innova Vascular, Inc. (1 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Innova Corp.?
FDA lists 6 510(k) clearances under the applicant name “Innova Corp.” (first 1991, 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 Innova Corp.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Innova Corp. is 47 days.
Which FDA product codes appear under Innova Corp.?
The most frequent FDA product codes under this applicant name are DZE (Implant, Endosseous, Root-Form, 4); LYG (Massager, Therapeutic, Manual, 1); MQN (External Mandibular Fixator And/Or Distractor, 1).
Next steps
- See all 6 Innova Corp. clearances with predicates and recalls
- Run predicate analysis for product code DZE, Innova Corp.'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.