Data / Medical devices / Canada / Arsci Inc.
Arsci Inc.: FDA-registered device maker in Longueuil Quebec, Canada, 1 510(k) clearance
Arsci Inc. is registered with the FDA (registration 3007293046) in Longueuil Quebec, Canada. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated April 19, 2011. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3007293046
- Address
- 982 Jean-Neveu, Longueuil Quebec, Canada, J4G 2M1
- Owner or operator
- ARSCI INC. (10041000)
- Roles
- Manufacturer
- First device listed
- June 11, 2012
- Registered through
- 2026
- Brand names listed
- ARSCI
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Microtools, Assisted Reproduction (Pipettes) | MQH | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| April 19, 2011 | K102480 | INJECTION PIPETTE; HOLDING PIPETTE; BIOPSY PIPETTE; DENUDING PIPETTE; PARTIAL ZONA DISSECTION (PZD) PIPETTE; ASSISTED HA | MQH | Substantially Equivalent | Jieying Laboratory, Inc. | accessdata.fda.gov |
Compare with other makers
Updated April 19, 2011. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.