Innovative Endoscopy Components, LLC.
Sunrise, FL, US
INNOVATIVE ENDOSCOPY COMPONENTS, LLC. appears in FDA device records in Sunrise, FL. FDA records list 3 510(k) clearances between and , 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 3 510(k) clearances for Innovative Endoscopy Components, LLC. between 1999 and 2008. The busiest year on record is 1999, with 1. The most recent is 2008, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1999 | 1 |
| 2006 | 1 |
| 2008 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K080809 | IEC MEDSIGHT AND MEDBRIGHT | FET | Substantially Equivalent | |
| K062707 | RUDOLF INNOVIEW AUTOCLAVABLE SEMI-RIGID URETERO-RENOSCOPE | FGB | Substantially Equivalent | |
| K992983 | BAHO AUTOCLAVABLE CYSTOSCOPE | FAJ | Substantially Equivalent |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 1064152 | 3002668781 | INNOVATIVE ENDOSCOPY COMPONENTS, LLC. | 320 International Pkwy, Sunrise, FL 33325 US | 2026 | No device listings on this registration |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain