Alara, Inc.: FDA filings under this applicant name
FDA lists 6 510(k) clearances under the applicant name “Alara, Inc.” (first 2000, latest 2011), across 2 product codes in 1 review panel. Median 510(k) review time under this name: 65 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 |
|---|---|---|---|
| MQB | Solid State X-Ray Imager (Flat Panel/Digital Imager) | 5 | 5 |
| KGI | Densitometer, Bone | 1 | 1 |
Review panels
- Radiology (6)
Most recent Alara, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K102479 | ALARA T210 COMPUTED RADIOGRAPHY SYSTEM | MQB | 2011-06-02 | 276 |
| K071682 | CRYSTALVIEW T-SERIES COMPUTED RADIOGRAPHY SYSTEM, MODELS T110 (WITH ERASER) AND T100 (WITHOUT ERASER) | MQB | 2007-08-15 | 57 |
| K062390 | CRYSTALVIEW R200 | MQB | 2006-09-18 | 33 |
| K061538 | ALARA CRYSTALVIEW COMPUTED RADIOGRAPHY SYSTEM, MODEL R200 | MQB | 2006-06-30 | 28 |
| K032210 | ALARA CRYSTALVIEW COMPUTED RADIOGRAPHY SYSTEM | MQB | 2003-10-02 | 73 |
| K000162 | METRISCAN BONE DENSITY SYSTEM | KGI | 2000-05-12 | 114 |
Recalls
openFDA lists no recalls under a recalling firm named Alara, 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.
Frequently asked questions
How many FDA 510(k) clearances are listed under Alara, Inc.?
FDA lists 6 510(k) clearances under the applicant name “Alara, Inc.” (first 2000, latest 2011), across 2 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 Alara, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Alara, Inc. is 65 days.
Which FDA product codes appear under Alara, Inc.?
The most frequent FDA product codes under this applicant name are MQB (Solid State X-Ray Imager (Flat Panel/Digital Imager), 5); KGI (Densitometer, Bone, 1).
Next steps
- See all 6 Alara, Inc. clearances with predicates and recalls
- Run predicate analysis for product code MQB, Alara, 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.