Identity
- Trade Name
- KIT EXPANDER EUDAMEDSURGICAL KIT FDA UDI
- Generic Name
- Dental/maxillofacial surgical procedure kit, non-medicated, reusable FDA UDI
- Device Name
- KIT (with exparder, Osteotome or Curette) EUDAMEDKIT BONE EXPANDER WITH STOPPER FDA UDI
- Model / Reference
- KEXP EUDAMEDFDA UDISURGICAL KIT EUDAMED
- Description
- KIT BONE EXPANDER WITH STOPPER FDA UDI
Identifiers
- Catalog Number
- KEXP FDA UDI
- Primary DI / UDI-DI
- 07899995209368 EUDAMEDFDA UDI
- Basic UDI-DI
- 999520000036K3 EUDAMED
- 510(k) Number
- K201688 FDA UDI
- FDA Product Code
- KCT FDA UDI
- EMDN Code
- L159016 DENTAL SURGERY INSTRUMENT KITS, REUSABLE EUDAMED
- GMDN Term
- Dental/maxillofacial surgical procedure kit, non-medicated, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 880.6850 FDA UDI
- Market of Registration
- Portugal EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
Single Use
No
Implantable
No
Reusable
Yes
Contains Latex
No
Reprocessed
Yes
CMR Substance
No
Human-derived
No
Human Tissues
No
Animal Tissues
No
Endocrine Disruptor
No
Administering Medicine
No
Measuring Function
No
Incorporates Medicinal Product
No
Prescription Use
Yes
Over-the-Counter
No
Convenience Kit
Yes
Combination Product
No
HCT/P
No
Premarket Exempt
No
Lot / Batch Number
Yes
Serial Number
Yes
Expiration Date
No
Manufacturing Date
Yes
Category: Dental/maxillofacial surgical procedure kit, non-medicated, reusable
Surgical Kit by S.I.N. - Sistema DE Implante Nacional S.A. — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
Similar devices
Also classified as Dental/maxillofacial surgical procedure kit, non-medicated, reusable.
- Dental Elevator Combo Set — SONTEC INSTRUMENTS, INC. · Class I
- Positioning Guide Full KIT — OSSTEM IMPLANT CO.,LTD · Class IIa
- Implantium, Superline — Dentium Co., Ltd. · Class I
- Bone Management — Hager & Meisinger Gesellschaft mit beschränkter Haftung · Class I
- Ditron Dental — DITRON DENTAL LTD · Class I
- KLOCKNER — SOADCO, S.L. · Class II
- HELMUT ZEPF — Helmut Zepf Medizintechnik GmbH · Class I
- Osteo KIT — OSSTEM IMPLANT Co., Ltd. · Class I
Cleared under the same submission
K201688 also covers:
- STERILIZATION BOX — S.I.N. - Sistema DE Implante Nacional S.A.
- STERILIZATION BOX — S.I.N. - Sistema DE Implante Nacional S.A.
- STERILIZATION BOX — S.I.N. - Sistema DE Implante Nacional S.A.
- STERILIZATION BOX — S.I.N. - Sistema DE Implante Nacional S.A.
- STERILIZATION BOX — S.I.N. - Sistema DE Implante Nacional S.A.
- STERILIZATION BOX — S.I.N. - Sistema DE Implante Nacional S.A.
- STERILIZATION BOX — S.I.N. - Sistema DE Implante Nacional S.A.
- STERILIZATION BOX — S.I.N. - Sistema DE Implante Nacional S.A.
- STERILIZATION BOX — S.I.N. - Sistema DE Implante Nacional S.A.
- SURGICAL INSTRUMENT — S.I.N. - Sistema DE Implante Nacional S.A.
- SURGICAL INSTRUMENT — S.I.N. - Sistema DE Implante Nacional S.A.
- SURGICAL INSTRUMENT — S.I.N. - Sistema DE Implante Nacional S.A.
Authorization Coverage (2 countries)
Regulatory Authorizations
MDR
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDR | — | Class II | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- S.I.N. - Sistema DE Implante Nacional S.A.
Sources (2)
- FDA UDI 2768f2cf-a26a-4ac3-b14f-890f442ae4ce 35 fields · synced Oct 7, 2026
- EUDAMED b13876be-f4f7-439d-a378-73a9e05e19a7 61 fields · synced Jul 9, 2026