Ultimate Wireforms, Inc.: FDA filings under this applicant name
FDA lists 6 510(k) clearances under the applicant name “Ultimate Wireforms, Inc.” (first 1992, latest 1996), across 2 product codes in 1 review panel. Median 510(k) review time under this name: 136 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 |
|---|---|---|---|
| DZC | Wire, Orthodontic | 5 | 5 |
| EAT | Tester, Pulp | 1 | 1 |
Review panels
- Dental (6)
Most recent Ultimate Wireforms, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K960799 | ORTHO-ICE | EAT | 1996-05-09 | 72 |
| K924805 | ORTHODONTIC ARCH WIRE | DZC | 1993-03-31 | 188 |
| K923837 | DIMPLED MULTI MODULUS ARCH WIRE | DZC | 1993-03-31 | 244 |
| K923836 | .016' X .016 NICKEL TITANIUM UPRIGHTING SPRING | DZC | 1992-12-23 | 146 |
| K923838 | THE ULTIMATE RCS ARCH WIRE | DZC | 1992-12-04 | 127 |
| K923839 | NITINOL GENTLE TOUCH COIL SPRING | DZC | 1992-10-15 | 77 |
Recalls
openFDA lists no recalls under a recalling firm named Ultimate Wireforms, 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.
- Ultimate Concepts, Inc. (3 510(k)s)
- Ultimate Development Corp. (1 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Ultimate Wireforms, Inc.?
FDA lists 6 510(k) clearances under the applicant name “Ultimate Wireforms, Inc.” (first 1992, latest 1996), 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 Ultimate Wireforms, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Ultimate Wireforms, Inc. is 136 days.
Which FDA product codes appear under Ultimate Wireforms, Inc.?
The most frequent FDA product codes under this applicant name are DZC (Wire, Orthodontic, 5); EAT (Tester, Pulp, 1).
Next steps
- See all 6 Ultimate Wireforms, Inc. clearances with predicates and recalls
- Run predicate analysis for product code DZC, Ultimate Wireforms, 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.