Cousin Biotech
WERVICQ-SUD Nord, FR
Cousin Biotech appears in FDA device records in WERVICQ-SUD Nord, FR. FDA records list one 510(k) clearance, no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.
FDA records held for this company
510(k) clearance history
FDA records hold 1 510(k) clearance for Cousin Biotech in 2007.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2007 | 1 |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 9616062 | 3003258310 | Cousin Biotech | ALLEE DES ROSES, WERVICQ-SUD Nord 59117 FR | 2026 | and 1 more, listed in full below |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
- KWPAppliance, Fixation, Spinal Interlaminal
- OWIBone Fixation Cerclage, Sublaminar
- JDQCerclage, Fixation
- OQLMesh, Surgical, Deployment Balloon
- FTLMesh, Surgical, Polymeric
- MNIOrthosis, Spinal Pedicle Fixation
- MNHOrthosis, Spondylolisthesis Spinal Fixation
- OSHPedicle Screw Spinal System, Adolescent Idiopathic Scoliosis
- GATSuture, Nonabsorbable, Synthetic, Polyethylene
- FTYTape, Measuring, Rulers And Calipers
- NKBThoracolumbosacral Pedicle Screw System
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
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Data as of , FDA export datePage updated Source: openFDA, public domain
