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Viky

FDA UDI

Class II (US FDA UDI)

by Endocontrol

Identity

Trade Name
VIKY FDA UDI
Generic Name
Surgical instrument assist arm system, power-adjusted FDA UDI
Model / Reference
AT0701 FDA UDI

Identifiers

Primary DI / UDI-DI
M975AT07011 FDA UDI
510(k) Number
K082233 FDA UDI
K122820 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Surgical instrument assist arm system, power-adjusted FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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

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 instrument assist arm system, power-adjusted

Viky by Endocontrol — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical instrument assist arm system, power-adjusted.

Cleared under the same submission

K082233 also covers:

K122820 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Endocontrol

Sources (1)

  • FDA UDI 681b54ad-6ae7-4186-9303-b33b82a03c44 34 fields · synced Jun 8, 2026