Renu Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Renu Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Reprocessed Tri Pulse Compression Garment
9
Total
9
Cleared
0
Denied
Renu Medical, Inc. has 9 FDA 510(k) cleared medical devices. Based in Everett, US.
Last cleared in 2021. Active since 2003. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Renu Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Renu Medical, Inc.
9 devices
Cleared
May 07, 2021
Reprocessed Tri Pulse Compression Garment
Cardiovascular
127d
Cleared
Jun 12, 2012
RENU MEDICAL REPROCESSED AIRCAST VENAFLOW CALF GARMENTS/ALL SIZES, RENU...
Cardiovascular
57d
Cleared
Nov 16, 2011
RENU MEDICAL REPROCESSED OXIMAX SENSORS: ADULT, PEDIATRIC, INFANT AND NEONATE
Anesthesiology
146d
Cleared
Jan 14, 2010
RENU MEDICAL VASOPRESS CALF , THIGH GARMENTS- ALL SIZESD, RENU MEDICAL...
Cardiovascular
50d
Cleared
Feb 06, 2009
RENU MEDICAL OXIMETRY SENSOR, ADULT, PED, INF,NEO
Anesthesiology
214d
Cleared
Nov 29, 2007
RENU REPROCESSED NELLCOR OXIMETRY SENSOR, MODEL D-25, N-25
Anesthesiology
114d
Cleared
May 25, 2007
RENU REPROCESSED NELLCOR OXYSENSOR, MODELS D-20 AND I-20
Anesthesiology
168d
Cleared
Apr 07, 2006
RENU MEDICAL REPROCESSED ALP 1 CALF GARMENT, MODEL ALP1
Cardiovascular
330d
Cleared
Nov 12, 2003
RENU MEDICAL REPORCESSED COMPRESSIBLE LIMB SLEEVES
Cardiovascular
177d