FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

Heylo™ System

K Number: K252140 · Decision Oct 6, 2025
Classifications
1
FEI Numbers
88
Registration Numbers
88
Same Product Code
101
Applicant Total
54
Review Days
90

Basic Information

Device Name
Heylo™ System
K Number
K252140
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
876.5900
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Coloplast Corp.
Date Received
July 8, 2025
Decision Date
October 6, 2025
Product Code
EXB
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
EXB Collector, Ostomy

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (EXB), ordered by most recent decision date.

View all

Other Clearances by Coloplast Corp.

K Number Device Name
K251116 Luja Coudé
K250270 Luja Set
K242049 SureCath Set
K241210 Luja Coude
K242173 Retrace Ureteral Access Sheath (ASXL10, ASXL12, ACXL10, ACXL12, AXXL10, AXXL12, ALXL10, ALXL12)
K242473 Altis Single Incision Sling System (519650); Aris Transobturator Sling System (519551); Supris Retropubic Sling System (519562)
K233411 Folysil Silicone Catheter
K231953 Biatain Fiber Ag (33570 - 5 cm x 5 cm / 2 in x 2 in); Biatain Fiber Ag (33572 - 10 cm x 12 cm / 4 in x 5 in); Biatain Fiber Ag (33574 - 15 cm x 15 cm / 6 in x 6 in); Biatain Fiber Ag (33576 - 2.5 cm x 46 cm / 1 in x 18 in); Biatain Fiber Ag (33578 - 20 cm x 30 cm / 8 in x 12 in)
K233101 Luja Coude (20108 Male CH18 - large packaging)
K213185 ImaJin Silicone double loop ureteral stent kits, ImaJin Pyelostent Silicone double loop ureteral stent kits, ImaJin Stenostent Silicone double loop ureteral stent kits
Search all 54 clearances from Coloplast Corp. →