Lares Manufacturing Co., Inc.: FDA filings under this applicant name
FDA lists 6 510(k) clearances under the applicant name “Lares Manufacturing Co., Inc.” (first 1978, latest 1983), across 4 product codes in 1 review panel. Median 510(k) review time under this name: 11 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 |
|---|---|---|---|
| EAY | Light, Fiber Optic, Dental | 2 | 2 |
| EFB | Handpiece, Air-Powered, Dental | 2 | 2 |
| EBF | Material, Tooth Shade, Resin | 1 | 1 |
| EIA | Unit, Operative Dental | 1 | 1 |
Review panels
- Dental (6)
Most recent Lares Manufacturing Co., Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K831351 | PERMALUX VISIBLE CURE COMPOSITE RESTOR | EBF | 1983-11-14 | 203 |
| K801535 | LARES HANDPIECE OIL | EFB | 1980-12-16 | 166 |
| K801592 | FIBER OPTIC HOSE | EAY | 1980-07-21 | 10 |
| K801591 | FIBER OPTIC ILLUMINATOR | EAY | 1980-07-21 | 10 |
| K801534 | LARES AIR PRESSURE GAUGE | EIA | 1980-07-14 | 11 |
| K780038 | DENTAL HANDPIECE | EFB | 1978-01-20 | 11 |
Recalls
openFDA lists no recalls under a recalling firm named Lares Manufacturing Co., 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.
- Lares Research, Inc. (10 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Lares Manufacturing Co., Inc.?
FDA lists 6 510(k) clearances under the applicant name “Lares Manufacturing Co., Inc.” (first 1978, latest 1983), across 4 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 Lares Manufacturing Co., Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Lares Manufacturing Co., Inc. is 11 days.
Which FDA product codes appear under Lares Manufacturing Co., Inc.?
The most frequent FDA product codes under this applicant name are EAY (Light, Fiber Optic, Dental, 2); EFB (Handpiece, Air-Powered, Dental, 2); EBF (Material, Tooth Shade, Resin, 1).
Next steps
- See all 6 Lares Manufacturing Co., Inc. clearances with predicates and recalls
- Run predicate analysis for product code EAY, Lares Manufacturing Co., 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.