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Ha Wildcat Fixed Length Total

FDA UDI

Class II (US FDA UDI)

by Grace Medical, Inc.

Identity

Trade Name
HA WILDCAT FIXED LENGTH TOTAL FDA UDI
Generic Name
Ossicular prosthesis, total FDA UDI
Device Name
HA WILDCAT FIXED LENGTH TOTAL 5.50MM LENGTH HA/TITANIUM FDA UDI
Model / Reference
708-550 FDA UDI
Description
HA WILDCAT FIXED LENGTH TOTAL 5.50MM LENGTH HA/TITANIUM FDA UDI

Identifiers

Primary DI / UDI-DI
00844505010382 FDA UDI
510(k) Number
K061853 FDA UDI
FDA Product Code
ETA FDA UDI
GMDN Term
Ossicular prosthesis, total FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.3495 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

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Ossicular prosthesis, total

Ha Wildcat Fixed Length Total by Grace Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ossicular prosthesis, total.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Grace Medical, Inc.

Sources (1)

  • FDA UDI 2cf7c391-bcae-4a77-9d91-28556734a7bd 35 fields · synced May 30, 2026