FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇸 Iceland

Kerecis Gingiva Graft

K Number: K192612 · Decision Nov 13, 2020
Classifications
1
FEI Numbers
57
Registration Numbers
57
Same Product Code
56
Applicant Total
10
Review Days
420

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Basic Information

Device Name
Kerecis Gingiva Graft
K Number
K192612
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3930
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Kerecis Limited
Date Received
September 20, 2019
Decision Date
November 13, 2020
Product Code
NPL
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

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

Product Code Device Name
NPL Barrier, Animal Source, Intraoral

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Other Clearances by Kerecis Limited

K Number Device Name
K251845 Marigen Wound Extra; Kerecis Silicone; Kerecis Parvus
K251844 Kerecis SurgiBind (50241)
K243843 Tendon Protect (50242)
K241080 Kerecis Parvus (50207)
K213231 Kerecis Silicone
K202430 Kerecis Reconstruct
K190528 MariGen Wound Extra
K153364 Kerecis SecureMesh
K132343 MARIGEN WOUND DRESSING