FDA cleared the VenAir, Sequential Compression System (9P-089000); VenAir, Sequential Compression System (PM01D01 / Calf garment (S)); VenAir, Sequential Compression System (PM01E01 / Calf garment (M)); VenAir, Sequential Compression System (PM01F01 / Calf garment (L)); VenAir, Sequential Compression System (PM01G01 / Thigh garment (S)); VenAir, Sequential Compression System (PM01H01 / Thigh garment (M)); VenAir, Sequential Compression System (PM01I01 / Thigh garment (L)); VenAir, Sequential Compr from Wellell, Inc. on Oct 28, 2025 under K251466, a special 510(k). The device falls under product code JOW, Sleeve, Limb, Compressible, regulated at 21 CFR 870.5800 as a Class 2 device. The review panel was Cardiovascular.
FDA logged the submission as received on May 13, 2025. The decision came 168 days later, longer than the 90 FDA-day review goal, which usually means at least one additional information request.
This is the only decision on file for Wellell, Inc. in the last 12 months of the tracker.
Questions & Answers
What did FDA clear under K251466?
K251466 is the FDA 510(k) for VenAir, Sequential Compression System (9P-089000); VenAir, Sequential Compression System (PM01D01 / Calf garment (S)); VenAir, Sequential Compression System (PM01E01 / Calf garment (M)); VenAir, Sequential Compression System (PM01F01 / Calf garment (L)); VenAir, Sequential Compression System (PM01G01 / Thigh garment (S)); VenAir, Sequential Compression System (PM01H01 / Thigh garment (M)); VenAir, Sequential Compression System (PM01I01 / Thigh garment (L)); VenAir, Sequential Compr, submitted by Wellell, Inc.. FDA's decision date was Oct 28, 2025, under product code JOW (Sleeve, Limb, Compressible).
Who makes the VenAir, Sequential Compression System (9P-089000); VenAir, Sequential Compression System (PM01D01 / Calf garment (S)); VenAir, Sequential Compression System (PM01E01 / Calf garment (M)); VenAir, Sequential Compression System (PM01F01 / Calf garment (L)); VenAir, Sequential Compression System (PM01G01 / Thigh garment (S)); VenAir, Sequential Compression System (PM01H01 / Thigh garment (M)); VenAir, Sequential Compression System (PM01I01 / Thigh garment (L)); VenAir, Sequential Compr?
Wellell, Inc., based in New Taipei City, is the applicant of record for K251466.
How long did the K251466 review take?
FDA received the submission on May 13, 2025 and issued its decision on Oct 28, 2025, 168 days later.