← Back to catalogue

Kincise™

FDA UDI

Class I (US FDA UDI)

by Synthes

Identity

Trade Name
KINCISE™ FDA UDI
Generic Name
Surgical power tool adaptor FDA UDI
Device Name
KINCISE POSTERIOR BROACH ADAPTER FDA UDI
Model / Reference
1010-01-101 FDA UDI
Description
KINCISE POSTERIOR BROACH ADAPTER FDA UDI

Identifiers

Catalog Number
1010-01-101 FDA UDI
Primary DI / UDI-DI
00845384018551 FDA UDI
FDA Product Code
GEY FDA UDI
GMDN Term
Surgical power tool adaptor FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical power tool adaptor

Kincise™ by Synthes — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical power tool adaptor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Synthes

Sources (1)

  • FDA UDI 0bf33ac4-00a4-408f-bffd-3d13fe1d2c53 36 fields · synced May 31, 2026