Integra® 90220
by Integra LifeSciences Production Corporation
Integra® 90220 is a Class II device made by Integra LifeSciences Production Corporation, cleared under FDA 510(k) K071218 on 14 Jun 2007 and listed in FDA GUDID since 21 Nov 2018 (UDI-DI 10381780510307), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number10381780510307 | Date21 Nov 2018 | StatusListed |
| United States | FDA 510(k)SESE | NumberK071218 | Date14 Jun 2007 | StatusActive |
Official records
- AccessGUDID record 10381780510307
- FDA 510(k) database K071218
Across registries
- FDA 510(k) K071218 decided 14 Jun 2007 Active
- FDA GUDID UDI-DI 10381780510307 listed 21 Nov 2018 Listed
Timeline
- Cleared FDA 510(k) K071218
- Listed FDA GUDID 10381780510307
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Integra®
- Generic name
- General-purpose light source
- Model / Ref / Catalog
- 90220
- Primary DI / UDI-DI
- 10381780510307
- 510(k) Number
- FDA product code
- FST
- GMDN term
- General-purpose light source
- Device class
- Class II
- Regulation number
- 878.4580
- GUDID distribution status
- In Commercial Distribution
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