RLS Interventional Inc. dba Inrad
Grand Rapids, MI, US
RLS Interventional Inc. DBA Inrad appears in FDA device records in Grand Rapids, MI. FDA records list no 510(k) clearances, no PMA records and one registered establishment. As of , FDA records show one recall for this company, and at least one establishment registration is current.
FDA records held for this company
FDA records under these names
1 nameFDA records resolved to RLS Interventional Inc. dba Inrad carry these names as well, as FDA wrote them. Each is the firm named on a registration, a 510(k), a PMA, a recall or an enforcement report that was joined to this company on a shared FDA identifier or on a matching name.
- Inrad, Increcall
510(k) clearance history
No 510(k) clearance records for this company in the ingested FDA data.
No 510(k) clearance records in the ingested FDA data.
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 1835568 | 3001237677 | RLS Interventional Inc. DBA Inrad | 4375 Donkers Ct SE, Grand Rapids, MI 49512 US | 2026 |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
Recall records
| Recall | Product | Reason | Classification | Initiated | Status |
|---|---|---|---|---|---|
| Z-1063-2011 | Inrad sample master aspiration biopsy needle with hiliter sharp bevel needle, 22 ga x 2 3/8'' (6 cm), model 41222, Inrad, Inc. Kentwood, MI. The device is intended for use during percutaneous biopsy and drainage procedures to obtain tissues or fluid specimens. | This lot of product has the wrong expiration date on the carton label. The pouches contained the correct expiration date. | Terminated |
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain