National Wire & Stamping, Inc.: FDA filings under this applicant name
FDA lists 5 510(k) clearances under the applicant name “National Wire & Stamping, Inc.” (first 1986, latest 1994), across 2 product codes in 2 review panels. Median 510(k) review time under this name: 58 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 |
|---|---|---|---|
| GEI | Electrosurgical, Cutting & Coagulation & Accessories | 4 | 4 |
| HGI | Electrocautery, Gynecologic (And Accessories) | 1 | 1 |
Review panels
Most recent National Wire & Stamping, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K940191 | ELECTROSURGICAL LOOP ELECTRODE | HGI | 1994-12-30 | 351 |
| K940192 | MIS ELECTROSURGICAL ELECTRODES | GEI | 1994-04-19 | 96 |
| K861595 | BALL ELECTRODES | GEI | 1986-06-19 | 51 |
| K861594 | ELECTROSURGICAL NEEDLE ELECTRODE (SOLID TYPE) | GEI | 1986-06-19 | 51 |
| K861495 | ELECTROSURGICAL BLADE ELECTRODE (SOLID TYPE) | GEI | 1986-06-19 | 58 |
Recalls
openFDA lists no recalls under a recalling firm named National Wire & Stamping, 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.
- National Medical Care, Medical Products Div., Inc. (62 510(k)s)
- National Patent Development Corp. (34 510(k)s)
- National Biological Corp. (28 510(k)s)
- National Custom Ent., Inc. (12 510(k)s)
- National Advanced Endoscopy Devices, Inc. (8 510(k)s)
- National Catheter Co. Div. Mallinckrodt (8 510(k)s)
- National Healthcare Mfg. Corp. (7 510(k)s)
- National Health-Care Equipment, Inc. (4 510(k)s)
- National Healthcare Linen Service (4 510(k)s)
- National Medical Technology (4 510(k)s)
- National Display Systems (3 510(k)s)
- National Hearing Aid Dist., Inc. (3 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under National Wire & Stamping, Inc.?
FDA lists 5 510(k) clearances under the applicant name “National Wire & Stamping, Inc.” (first 1986, latest 1994), across 2 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 National Wire & Stamping, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name National Wire & Stamping, Inc. is 58 days.
Which FDA product codes appear under National Wire & Stamping, Inc.?
The most frequent FDA product codes under this applicant name are GEI (Electrosurgical, Cutting & Coagulation & Accessories, 4); HGI (Electrocautery, Gynecologic (And Accessories), 1).
Next steps
- See all 5 National Wire & Stamping, Inc. clearances with predicates and recalls
- Run predicate analysis for product code GEI, National Wire & Stamping, 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.