Data / Medical devices / Mexico / AVENT S. de R.L. de C.V.
AVENT S. de R.L. de C.V.: FDA-registered device maker in NOGALES Sonora, Mexico, 37 510(k) clearances
AVENT S. de R.L. de C.V. is registered with the FDA (registration 9611594) in NOGALES Sonora, Mexico. It lists 19 device types. The FDA files 37 510(k) clearances under its listings, the newest dated October 25, 2024. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 9611594
- FEI number
- 3002806436
- Address
- Circuito Industrial No.40 Colonia Obrera, NOGALES Sonora, Mexico, CP 84048
- Owner or operator
- Avanos Medical, Inc. (2022573)
- Roles
- Manufacturer, Repackager or relabeler, Specification developer
- First device listed
- April 11, 2006
- Registered through
- 2026
- Brand names listed
- ANTI-FOG KIT, BALLARD, BD Epilor™ Plastic LOR 7 mL with luer slip tip syringe, Ballard Metered Dose Inhaler (MDI) Adapter, Ballard Single Dose Vials, 0.9% Sodium Chloride Solution, Busse EpiGlide Loss of Resistance LOR Syringe, CORFLO* PEG Kit, CORGRIP* SR NG/NI Tube Retention System and more
Devices it lists
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| October 25, 2024 | K241185 | CORGRIP* SR NG/NI Tube Retention System | KNT | Substantially Equivalent | Avanos Medical, Inc. | accessdata.fda.gov |
| June 6, 2024 | K240965 | CORTRAK* 2 Enteral Access System (20-0950) | KNT | Substantially Equivalent | Avanos Medical, Inc. | accessdata.fda.gov |
| May 19, 2022 | K210983 | BD Epilor Syringe | CAZ | Substantially Equivalent | Becton, Dickinson and Company | accessdata.fda.gov |
| April 22, 2022 | K220588 | Avanos* CORTRAK* 2 Enteral Access System (EAS) | KNT | Substantially Equivalent | Avanos Medical, Inc. | accessdata.fda.gov |
| May 4, 2017 | K162254 | Cedic Enteral ENFit Transition Connectors | PIO | Substantially Equivalent | Cedic S.R.L. | accessdata.fda.gov |
| March 26, 2014 | K133599 | CORGRIP | KNT | Substantially Equivalent | Corpak Medsystems | accessdata.fda.gov |
| June 26, 2013 | K122653 | MIC-KEY SF LOW PROFILE GASTROSTOMY TUBE AND ACCESSORIES | KNT | Unknown | Kimberly-Clark Corporation | accessdata.fda.gov |
| May 11, 2012 | K113333 | KIMBERLY-CLARK KIM VENT MICROCUFF ENDOTRACHEAL TUBE FOR ADULTS | BTR | Substantially Equivalent | Kimberly-Clark Corporation | accessdata.fda.gov |
| January 10, 2012 | K113351 | CORTRAK ENTERAL ACCESS DEVICE | KNT | Substantially Equivalent | Corpak Medsystems | accessdata.fda.gov |
| August 3, 2010 | K100288 | NEOMED ENTERAL ONLY EXTENSION SET | KNT | Substantially Equivalent | Neomed, Inc. | accessdata.fda.gov |
| December 8, 2009 | K093312 | KIMBERLY-CLARK GASTROINTESTINAL ANCHOR SET WITH SAF-T-PEXY FASTENERS, ENTERNAL ACCESS DILATION SYSTEM | KGC | Substantially Equivalent | Kimberly-Clark Corp. | accessdata.fda.gov |
| December 29, 2008 | K083210 | CORFLO ANTI IV ENTERAL FEEDING TUBE | FPD | Substantially Equivalent | Corpak Medsystems | accessdata.fda.gov |
| July 9, 2008 | K080804 | BUSSE PLASTIC LOR SYRINGE | CAZ | Substantially Equivalent | Busse Hosipital Disposables | accessdata.fda.gov |
| February 26, 2008 | K080253 | KIMBERLY-CLARK INTRODUCER KITS | KGC | Unknown | Kimberly-Clark Corp. | accessdata.fda.gov |
| May 6, 2005 | K043044 | ANTI-I.V. ENTERAL FEEDING SYSTEM | KNT | Substantially Equivalent | Viasys Medsystems | accessdata.fda.gov |
| December 10, 2004 | K043114 | KIMBERLY-CLARK MIC-KEY LOW PROFILE GASTROSTOMY TUBE | KNT | Substantially Equivalent | Kimberly-Clark Corp. | accessdata.fda.gov |
| March 31, 2003 | K030721 | QUICK-TAP PARACENTESIS TRAY, KIT & NEEDLE | LRO | Substantially Equivalent | Ballard Medical Products | accessdata.fda.gov |
| June 9, 2000 | K001287 | EMPTY RESERVOIR BAG, 50 ML,100 ML,250 ML,500 ML, 1000M ML, 1500 ML, 2000 ML, 3000 ML | KPE | Substantially Equivalent | Sorenson Medical, Inc. | accessdata.fda.gov |
| October 20, 1999 | K993138 | BALLARD MIC-KEY G LOW PROFILE GASTROSTOMY REPLACEMENT KIT | KNT | Substantially Equivalent | Ballard Medical Products | accessdata.fda.gov |
| September 11, 1998 | K982894 | MIC-KEY GLOW PROFILE GASTROSTOMY REPLACEMENT KIT | KNT | Substantially Equivalent | Ballard Medical Products | accessdata.fda.gov |
| October 8, 1996 | K962042 | GLASS SYRINGE | FMF | Substantially Equivalent | Ispg, Inc. | accessdata.fda.gov |
| September 28, 1994 | K926581 | MIC TRANSGASTRIC JEJUNAL TUBE | KNT | Substantially Equivalent | Medical Innovations Corp. | accessdata.fda.gov |
| August 5, 1994 | K941464 | BASICS ENDOSCOPY SYSTEM | OCZ | Substantially Equivalent | Cox Medical Ent., Inc. | accessdata.fda.gov |
| May 26, 1994 | K941562 | 1ML LUER-LOK SYRINGE | FMF | Substantially Equivalent | Bd Becton Dickinson Vacutainer Systems Preanalytic | accessdata.fda.gov |
| May 2, 1994 | K921652 | MIC TRANSGASTRIC JEJUNAL FEEDING TUBE KIT | KNT | Unknown | Medical Innovations Corp. | accessdata.fda.gov |
| May 2, 1994 | K921370 | MIC GASTRO-ENTEROSTOMY TUBE MODIFICATION | KNT | Unknown | Medical Innovations Corp. | accessdata.fda.gov |
| April 29, 1994 | K940431 | TECNADYNE 20/20 FOG INHIBITOR KIT | GCJ | Substantially Equivalent | Tecnadyne Scientific, Inc. | accessdata.fda.gov |
| February 17, 1994 | K924065 | MIC PEG TUBE | KNT | Unknown | Medical Innovations Corp. | accessdata.fda.gov |
| December 1, 1993 | K922667 | MIC LOW PROFILE GASTROSTOMY TUBE | KNT | Unknown | Medical Innovations Corp. | accessdata.fda.gov |
| September 21, 1988 | K882867 | CORPAK PERCUTANEOUS ENDOSCOPIC GASTROSTOMY TUBE | KNT | Substantially Equivalent | Corpak Co. | accessdata.fda.gov |
| August 22, 1985 | K853197 | MIC JEJUNAL FEEDING TUBE | KNT | Substantially Equivalent | Medical Innovations Corp. | accessdata.fda.gov |
| August 14, 1985 | K852707 | GASTRO-ENTEROSTOMY TUBE | KNT | Substantially Equivalent | Medical Innovations Corp. | accessdata.fda.gov |
| January 7, 1985 | K844745 | K-TUBE | KNT | Substantially Equivalent | Midwest Metabolic Support Group | accessdata.fda.gov |
| August 14, 1984 | K842076 | MIC GASTROSTOMY TUBE | KNT | Substantially Equivalent | Medical Innovations Corp. | accessdata.fda.gov |
| June 11, 1984 | K842115 | SPUNGARD & SURG. DRAPES-GOWNS & PACKS | KKX | Substantially Equivalent | Kimberly-Clark Corp. | accessdata.fda.gov |
| July 19, 1983 | K831328 | NEONATAL NASOGASTRIC FEEDING TUBE- | KNT | Substantially Equivalent | Corpak Medsystems | accessdata.fda.gov |
| July 13, 1982 | K821906 | CORPAK ENTERIC FEEDING TUBE W/GUIDE TIP | KNT | Substantially Equivalent | Corpak Medsystems | accessdata.fda.gov |
Compare with other makers
- All makers of Tubes, Gastrointestinal (And Accessories)
- All makers of Enteral Specific Transition Connectors
- All makers of Drape, Surgical, Antimicrobial
- All makers of Tube, Gastro-Enterostomy
- All makers of Tape And Bandage, Adhesive, Adjustable Closing Mechanism, Otc Use
- All makers of Accessories, Cleaning Brushes, For Endoscope
Updated October 25, 2024. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.