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Partial Thickness Sponge

FDA UDI

Class II (US FDA UDI)

by Labtician Ophthalmics, Inc

Identity

Trade Name
Partial Thickness Sponge FDA UDI
Generic Name
Scleral buckling device, bioabsorbable FDA UDI
Model / Reference
S 1984-7.5 FDA UDI

Identifiers

Primary DI / UDI-DI
10871321001451 FDA UDI
510(k) Number
K875014 FDA UDI
FDA Product Code
HQJ FDA UDI
GMDN Term
Scleral buckling device, bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.3300 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Scleral buckling device, bioabsorbable

Partial Thickness Sponge by Labtician Ophthalmics, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Scleral buckling device, bioabsorbable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1d5ad5eb-3730-4bb8-9083-280b6a8f4704 34 fields · synced Jun 8, 2026