Ndm Corp.: FDA filings under this applicant name
FDA lists 11 510(k) clearances under the applicant name “Ndm Corp.” (first 1976, latest 1993), across 7 product codes in 4 review panels. Median 510(k) review time under this name: 25 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 |
|---|---|---|---|
| DRX | Electrode, Electrocardiograph | 3 | 3 |
| GEI | Electrosurgical, Cutting & Coagulation & Accessories | 3 | 3 |
| FOZ | Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days | 1 | 1 |
| GXY | Electrode, Cutaneous | 1 | 1 |
| HAM | Apparatus, Electrosurgical | 1 | 1 |
| JOS | Electrode, Electrosurgical | 1 | 1 |
| NAE | Dressing, Wound, Hydrogel Without Drug And/Or Biologic | 1 | 1 |
Review panels
Most recent Ndm Corp. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K926202 | CLEARSITE STERILE WOUND DRESSING, NDM WOUND DRESSI | NAE | 1993-05-12 | 154 |
| K901145 | NDM SWITCHPEN HOLSTER | GEI | 1990-05-09 | 58 |
| K853968 | DIATEMP ELECTROSURGICAL PEN | GEI | 1985-11-14 | 49 |
| K830663 | PENCIL SKIN ABRADER | DRX | 1983-04-28 | 56 |
| K810920 | NDM DIATEMP INFANT ELECTROSURG. DISP. P. | HAM | 1981-05-01 | 25 |
| K801158 | NDM DIATEMP ELECTROSURGICAL DIS. PAD | GEI | 1980-05-23 | 9 |
| K790730 | NDM PAPER TAPE ECG ELECTRODE | DRX | 1979-04-26 | 13 |
| K772354 | I.V. CATHETER | FOZ | 1978-01-31 | 35 |
| K772160 | ELECTROSURGICAL GROUNDING PAD | JOS | 1977-11-28 | 12 |
| K761301 | V-TRACE ECG BACKPAD | DRX | 1977-01-05 | 14 |
1 earlier clearances. See the full list in Caduvo.
Recalls
openFDA lists no recalls under a recalling firm named Ndm 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.
Frequently asked questions
How many FDA 510(k) clearances are listed under Ndm Corp.?
FDA lists 11 510(k) clearances under the applicant name “Ndm Corp.” (first 1976, latest 1993), across 7 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 Ndm Corp.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Ndm Corp. is 25 days.
Which FDA product codes appear under Ndm Corp.?
The most frequent FDA product codes under this applicant name are DRX (Electrode, Electrocardiograph, 3); GEI (Electrosurgical, Cutting & Coagulation & Accessories, 3); FOZ (Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days, 1).
Next steps
- See all 11 Ndm Corp. clearances with predicates and recalls
- Run predicate analysis for product code DRX, Ndm 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.