Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Renu Medical with 9 510(k) clearances. The most recent is a 510(k) clearance dated May 7, 2021: Reprocessed Tri Pulse Compression Garment.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| May 7, 2021 | Reprocessed Tri Pulse Compression GarmentK203847 · JOW | 510(k) clearances |
| Jun 12, 2012 | RENU MEDICAL REPROCESSED AIRCAST VENAFLOW CALF GARMENTS/ALL SIZES, RENU MEDICAL REPROCESSED AIRCAST VENAFLOW THIGH GARMEK121145 · JOW | 510(k) clearances |
| Nov 16, 2011 | RENU MEDICAL REPROCESSED OXIMAX SENSORS: ADULT, PEDIATRIC, INFANT AND NEONATEK111773 · NLF | 510(k) clearances |
| Jan 14, 2010 | RENU MEDICAL VASOPRESS CALF , THIGH GARMENTS- ALL SIZESD, RENU MEDICAL VASOPRESS FOOT GARMENTSK093658 · JOW | 510(k) clearances |
| Feb 6, 2009 | RENU MEDICAL OXIMETRY SENSOR, ADULT, PED, INF,NEOK081927 · NLF | 510(k) clearances |
| Nov 29, 2007 | RENU REPROCESSED NELLCOR OXIMETRY SENSOR, MODEL D-25, N-25K072194 · NLF | 510(k) clearances |
| May 25, 2007 | RENU REPROCESSED NELLCOR OXYSENSOR, MODELS D-20 AND I-20K063661 · NLF | 510(k) clearances |
| Apr 7, 2006 | RENU MEDICAL REPROCESSED ALP 1 CALF GARMENT, MODEL ALP1K051227 · JOW | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
