Adel Medical , Ltd.: FDA filings under this applicant name
FDA lists 8 510(k) clearances under the applicant name “Adel Medical , Ltd.” (first 1980, latest 1989), across 5 product codes in 3 review panels. Median 510(k) review time under this name: 33 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 |
|---|---|---|---|
| KNC | Table, Obstetric (And Accessories) | 3 | 3 |
| HDD | Table, Obstetrical, Ac-Powered (And Accessories) | 2 | 2 |
| FMR | Device, Transfer, Patient, Manual | 1 | 1 |
| FMZ | Incubator, Neonatal | 1 | 1 |
| FSS | Light, Surgical, Floor Standing | 1 | 1 |
Review panels
Most recent Adel Medical , Ltd. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K890476 | ADEL - MODEL 986 INFANT WARMER | FMZ | 1989-06-16 | 136 |
| K874610 | ADEL MODEL 2100 BIRTHING BED | HDD | 1988-01-21 | 73 |
| K871475 | SOLOLIFT - PATIENT TRANSFER STRETCHER | FMR | 1987-05-11 | 27 |
| K861030 | LABOR-DELIVERY STRETCH/BED | KNC | 1986-04-23 | 36 |
| K860020 | MINOR SURGERY LIGHT MODEL 2112 | FSS | 1986-01-24 | 21 |
| K833321 | LABOR/DELIVERY/RECOVERY BED LDR-600 | KNC | 1983-11-14 | 49 |
| K810886 | ADEL MEDICAL BIRTHING BED, #LD-500 | HDD | 1981-04-23 | 22 |
| K801622 | ADEL MEDICAL BIRTHING BED, MOD. LD-400 | KNC | 1980-08-14 | 30 |
Recalls
openFDA lists no recalls under a recalling firm named Adel Medical , 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 Adel Medical , Ltd.?
FDA lists 8 510(k) clearances under the applicant name “Adel Medical , Ltd.” (first 1980, latest 1989), across 5 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 Adel Medical , Ltd.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Adel Medical , Ltd. is 33 days.
Which FDA product codes appear under Adel Medical , Ltd.?
The most frequent FDA product codes under this applicant name are KNC (Table, Obstetric (And Accessories), 3); HDD (Table, Obstetrical, Ac-Powered (And Accessories), 2); FMR (Device, Transfer, Patient, Manual, 1).
Next steps
- See all 8 Adel Medical , Ltd. clearances with predicates and recalls
- Run predicate analysis for product code KNC, Adel Medical , 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.