FDA Registration
Active
🇬🇧 United Kingdom
1120720
Reg #: 9614209
·
FEI: 3002806725
·
Expires 2025
Products
1
Proprietary Names
103
Establishment Types
2
Classifications
1
Registration Details
- Registration Name
- CORIN LTD.
- Registration Number
- 9614209
- FEI Number
- 3002806725
- Status
- Active
- Expiry Year
- 2025
- Initial Importer
- No
- Address
- THE CORINIUM CENTRE
- City
- CIRENCESTER Gloucestershire
- Country
- GB
Regulatory Submissions
- 510(k) Number
- K240875
Owner / Operator
- Firm Name
- CORIN LTD.
- Operator Number
- 9012268
- Address
- THE CORINIUM CENTRE, --
- City
- CIRENCESTER
- State
- Gloucestershire
- Postal Code
- GL7 1YJ
- Country
- GB
- Correspondent
- Lucinda A Gerber
US Agent
- Business Name
- OMNIlifeScience, Inc.
- Contact Name
- Lucinda Gerber
- Address
- 480 Paramount Dr
- City
- Raynham
- State
- MA
- ZIP
- 02767
- Country
- US
- [email protected]
- Phone
- 772 3212478
Products
| Device Name | Product Code | Device Class | Medical Specialty | Exempt | Created |
|---|---|---|---|---|---|
| Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | JWH | Class 2 | Orthopedic | No | 2024-07-03 |
Proprietary Names
1120720
1120772
1120814
1120109
1120920
1120114
1120861
1120862
1120410
1120716
1120768
1120718
1120616
1120764
1120511
1120914
1120322
1120612
1120812
1120211
1120622
1120610
1120918
1120766
1120122
1120312
1120422
1120411
1120214
1120711
1120222
1120811
1120418
1120810
1120722
1120320
1120820
1120912
1120212
1233703
1120116
1120866
1120518
1120309
1120314
1120412
1120909
1120809
1120868
1120859
1120712
1120414
1120922
1120770
1120118
1120618
1120864
1120759
1120860
1120210
1120710
1120218
1120420
1120520
1120510
1120310
1120916
1120311
1120816
1120714
1120112
1120514
1120911
1120761
1120762
1120409
1120709
1120209
1120216
1120316
1233702
1120611
1120870
1120120
1120220
1120760
1120111
1120416
1120516
1120818
1120509
1120620
1233701
1120318
1120910
1120512
1120609
1120614
1120110
1120822
1120872
1120522
1233791
Establishment Types
Complaint File Establishment per 21 CFR 820.198
Manufacture Medical Device