Identity
- Trade Name
- EPIPHANY FDA UDI
- Generic Name
- Bone curette, reusable FDA UDI
- Device Name
- 18MM CURVED 30 DEGREE DOWN COBB SHAFT FDA UDI
- Model / Reference
- 1 FDA UDI
- Description
- 18MM CURVED 30 DEGREE DOWN COBB SHAFT FDA UDI
Identifiers
- Catalog Number
- 1001-1802 1022-14 FDA UDI
- Primary DI / UDI-DI
- B528100118021022140 FDA UDI
- 510(k) Number
- K113781 FDA UDI
- FDA Product Code
- MAX FDA UDI
- GMDN Term
- Bone curette, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3080 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Height — 18 Millimeter FDA UDIAngle — 30 degree FDA UDI
Category: Bone curette, reusable
Epiphany by Pantheon Spinal LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Volkmann Bone Curette Oval - Fig. 00 17 cm - 6 3/4" Scoop Size 4.4 mm Stainless Steel — SURTEX INSTRUMENTS LTD · Class I
Cleared under the same submission
K113781 also covers:
- EPIPHANY — Pantheon Spinal LLC
- EPIPHANY — Pantheon Spinal LLC
- EPIPHANY — Pantheon Spinal LLC
- EPIPHANY — Pantheon Spinal LLC
- EPIPHANY — Pantheon Spinal LLC
- EPIPHANY — Pantheon Spinal LLC
- EPIPHANY — Pantheon Spinal LLC
- EPIPHANY — Pantheon Spinal LLC
- EPIPHANY — Pantheon Spinal LLC
- EPIPHANY — Pantheon Spinal LLC
- EPIPHANY — Pantheon Spinal LLC
- EPIPHANY — Pantheon Spinal LLC
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| 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
- Pantheon Spinal LLC
Sources (1)
- FDA UDI 9c9dc2ba-f542-4340-80b5-de94ba545c25 37 fields · synced May 31, 2026