Dmp, Ltd.: FDA filings under this applicant name
FDA lists 9 510(k) clearances under the applicant name “Dmp, Ltd.” (first 1989, latest 2012), across 5 product codes in 2 review panels. Median 510(k) review time under this name: 101 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 | 1 | 88 |
| 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 |
|---|---|---|---|
| EBF | Material, Tooth Shade, Resin | 3 | 3 |
| LYY | Latex Patient Examination Glove | 3 | 3 |
| EBC | Sealant, Pit And Fissure, And Conditioner | 1 | 1 |
| ELW | Material, Impression | 1 | 1 |
| KLE | Agent, Tooth Bonding, Resin | 1 | 1 |
Review panels
- Dental (6)
- General Hospital (3)
Most recent Dmp, Ltd. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K121915 | BRIGHT RESTORATIVE MATERIALS | EBF | 2012-09-28 | 88 |
| K102836 | BONASIL A+ IMPRESSION MATERIALS | ELW | 2011-01-13 | 106 |
| K102252 | DMP PIT & FISSURE SEALANT | EBC | 2010-12-03 | 115 |
| K102255 | DMP ETCHING GEL | EBF | 2010-11-23 | 105 |
| K102254 | DMP SINGLE BONDING | KLE | 2010-11-23 | 105 |
| K102257 | NANOCERAM- BRIGHT | EBF | 2010-11-19 | 101 |
| K892965 | LATEX EXAM GLOVES (MFG. BROADLAND RUBBER INDUST.) | LYY | 1989-06-14 | 63 |
| K892150 | PATIENT EXAMINATION GLOVES (LATEX) | LYY | 1989-06-06 | 62 |
| K891661 | PATIENT EXAMINATION GLOVES (LATEX) | LYY | 1989-05-25 | 66 |
Recalls
openFDA lists no recalls under a recalling firm named Dmp, Ltd..
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 Dmp, Ltd.?
FDA lists 9 510(k) clearances under the applicant name “Dmp, Ltd.” (first 1989, latest 2012), across 5 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 Dmp, Ltd.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Dmp, Ltd. is 101 days.
Which FDA product codes appear under Dmp, Ltd.?
The most frequent FDA product codes under this applicant name are EBF (Material, Tooth Shade, Resin, 3); LYY (Latex Patient Examination Glove, 3); EBC (Sealant, Pit And Fissure, And Conditioner, 1).
Next steps
- See all 9 Dmp, Ltd. clearances with predicates and recalls
- Run predicate analysis for product code EBF, Dmp, Ltd.'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.