FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

BTL-785NEH

K Number: K253750 · Decision Mar 17, 2026
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
42
Review Days
112

Basic Information

Device Name
BTL-785NEH
K Number
K253750
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
BTL Industries, Inc.
Date Received
November 25, 2025
Decision Date
March 17, 2026
Product Code
GEI
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

Similar 510(k) Clearances

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

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Other Clearances by BTL Industries, Inc.

K Number Device Name
K252963 BTL-899TT
K252561 BTL-754FF
K250309 BTL-199
K243290 BTL-785MJ
K241516 BTL-398
K241270 BTL-754
K242532 BTL-785BNF-E
K240234 BTL-899MS
K233849 BTL-499
K233604 BTL-785S
Search all 42 clearances from BTL Industries, Inc. →