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Finesse Sharkskin

FDA UDIEUDAMED

Class I (US FDA UDI)

by Alcon Laboratories, Inc.

Identity

Trade Name
FINESSE SHARKSKIN FDA UDI
Generic Name
Ophthalmic soft-tissue surgical forceps probe-tip, single-use FDA UDI
Device Name
23G Adv DSP Tip FINESSE™ SHARKSKIN™ ILM Forceps FDA UDI
Model / Reference
07612717071759 FDA UDI
Description
23G Adv DSP Tip FINESSE™ SHARKSKIN™ ILM Forceps FDA UDI

Identifiers

Primary DI / UDI-DI
07612717071759 FDA UDI
FDA Product Code
HNR FDA UDI
GMDN Term
Ophthalmic soft-tissue surgical forceps probe-tip, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4350 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Ophthalmic soft-tissue surgical forceps probe-tip, single-use

Finesse Sharkskin by Alcon Laboratories, Inc. — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic soft-tissue surgical forceps probe-tip, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Alcon Laboratories, Inc.

Sources (2)

  • FDA UDI aa22919f-502f-4962-a62a-5b62170664ef 33 fields · synced Jun 19, 2026
  • EUDAMED 1 fields · synced Jun 3, 2026