← Back to catalogue

Epsilon USA

FDA UDI

Class I (US FDA UDI)

by Epsilon Eye Care Private Limited

Identity

Trade Name
Epsilon USA FDA UDI
Generic Name
Ophthalmic suture scissors FDA UDI
Device Name
Corneal Full Curved Scissors (97.5 mm overall) Titanium FDA UDI
Model / Reference
ES-10 FDA UDI
Description
Corneal Full Curved Scissors (97.5 mm overall) Titanium FDA UDI

Identifiers

Primary DI / UDI-DI
G346ES100 FDA UDI
FDA Product Code
HNF FDA UDI
GMDN Term
Ophthalmic suture scissors 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Ophthalmic suture scissors

Epsilon USA's Corneal Full Curved Scissors are a high-performance, hand-held ophthalmic surgical instrument designed for cutting sutures during eye surgery. Made from high-grade stainless steel, these scissors feature pivoted blades with finger and thumb rings for a precise shearing action.

Similar devices

Also classified as Ophthalmic suture scissors.

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

Sources (1)

  • FDA UDI 654c8099-c1c2-41ff-96ce-3f5e45b15b1c 34 fields · synced Jul 18, 2026