A.D.T. Lab Industries: FDA filings under this applicant name
FDA lists 21 510(k) clearances under the applicant name “A.D.T. Lab Industries” (first 1980, latest 1981), across 6 product codes in 3 review panels. Median 510(k) review time under this name: 28 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 |
|---|---|---|---|
| GAA | Needle, Aspiration And Injection, Disposable | 14 | 14 |
| FCG | Biopsy Needle | 3 | 3 |
| FSM | Tray, Surgical, Instrument | 1 | 1 |
| GBW | Catheter, Peritoneal | 1 | 1 |
| GDM | Needle, Aspiration And Injection, Reusable | 1 | 1 |
| KMJ | Lubricant, Patient | 1 | 1 |
Review panels
Most recent A.D.T. Lab Industries 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K812297 | A.D.T. PROCEDURES TRAY | KMJ | 1981-09-28 | 45 |
| K801754 | ADT BONE MARROW ASPIRATION NEEDLE | GAA | 1980-08-20 | 23 |
| K801753 | ADT BONE MARROW BIOPSY-ASPIR. NEELDE | GAA | 1980-08-20 | 23 |
| K800418 | ADT DISPOSABLE THIN NEEDLE ASPIRATION | FSM | 1980-04-28 | 62 |
| K800417 | ADT PTC PRO. TRAY W/(SKINNY CHIBA) NEEDL | GAA | 1980-04-28 | 62 |
| K800414 | ADT SOFT TISSUE BIOPSY TRAY | GAA | 1980-04-28 | 62 |
| K800412 | ROSENTHAL NEEDLE (DISP.) ADT BONE MARROW | GAA | 1980-04-28 | 62 |
| K800411 | ASPIRATION TRAY W/FERRIS DISP. ILLINOIS | GAA | 1980-04-28 | 62 |
| K800410 | ADT BONE MARROW BIOPSY-ASPIRATION TRAY | GAA | 1980-04-28 | 62 |
| K800409 | ADT BONE MARROW BIOPSY ASPIRATION TRAY | GAA | 1980-04-28 | 62 |
11 earlier clearances. See the full list in Caduvo.
Recalls
openFDA lists no recalls under a recalling firm named A.D.T. Lab Industries.
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 A.D.T. Lab Industries?
FDA lists 21 510(k) clearances under the applicant name “A.D.T. Lab Industries” (first 1980, latest 1981), across 6 product codes in 3 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 A.D.T. Lab Industries?
The median time from FDA receipt to decision across 510(k)s cleared under the name A.D.T. Lab Industries is 28 days.
Which FDA product codes appear under A.D.T. Lab Industries?
The most frequent FDA product codes under this applicant name are GAA (Needle, Aspiration And Injection, Disposable, 14); FCG (Biopsy Needle, 3); FSM (Tray, Surgical, Instrument, 1).
Next steps
- See all 21 A.D.T. Lab Industries clearances with predicates and recalls
- Run predicate analysis for product code GAA, A.D.T. Lab Industries'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.