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Sign in to claim this brandTRINITY STERILE, INC.
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 201 Kiley Dr, SALISBURY, MD, 21801
- Website
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- —
- —
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- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 1000123297
- DUNS Number
- —
Catalogue (390)
Page 6 of 8| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Trinity Sterile, Inc. | T97-771 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 81393B | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 80362 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 2270A | FDA UDI | N | Active |
| Trinity Sterile, Inc. | 2290A | FDA UDI | N | Active |
| Trinity Sterile, Inc. | 10004 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | T98-494 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | T98-482 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 6089 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 6049 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 50378 | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | 81454 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 50264 | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | 50383 | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | 5013 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 94-1924 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 50668 | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | 80361 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 6042 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 5088 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 7018 | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | 6036 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 81393 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 85287UMMC | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | 96-4137M | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 20653 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 5047 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 22102 | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | T98-489 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 50390KP | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | 50246 | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | 50848 | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | 85378 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 81371 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 20210 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 5079 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 86115 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 10007 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 7088 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 7008 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 86122 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 81250 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 50518 | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | 82027 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 6037 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 20652 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 50690 | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | 5000 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 81651 | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | 7031 | FDA UDI | Class I | Active |
Related Companies
Authorised Representatives
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Importers
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Notified Bodies
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Authorities
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FDA Recalls (10)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Dec 13, 2024 | Z-1012-2025 | — | open, classified | Potential for hole in package compromising sterility of the medical kit. |
| Dec 13, 2024 | Z-1016-2025 | — | open, classified | Potential for hole in package compromising sterility of the medical kit. |
| Dec 13, 2024 | Z-1015-2025 | — | open, classified | Potential for hole in package compromising sterility of the medical kit. |
| Dec 13, 2024 | Z-1013-2025 | — | open, classified | Potential for hole in package compromising sterility of the medical kit. |
| Dec 13, 2024 | Z-1014-2025 | — | open, classified | Potential for hole in package compromising sterility of the medical kit. |
| Jun 29, 2022 | Z-1551-2022 | — | terminated | Kits mislabeled as latex-free, the packaging for component 94-7002 Non-Adherent Dressing contains natural rubber latex. Potential risk to to those with latex allergy |
| Jun 29, 2022 | Z-1548-2022 | — | terminated | Kits mislabeled as latex-free, the packaging for component 94-7002 Non-Adherent Dressing contains natural rubber latex. Potential risk to to those with latex allergy |
| Jun 29, 2022 | Z-1550-2022 | — | terminated | Kits mislabeled as latex-free, the packaging for component 94-7002 Non-Adherent Dressing contains natural rubber latex. Potential risk to to those with latex allergy |
| Jun 29, 2022 | Z-1549-2022 | — | terminated | Kits mislabeled as latex-free, the packaging for component 94-7002 Non-Adherent Dressing contains natural rubber latex. Potential risk to to those with latex allergy |
| Feb 23, 2021 | Z-1468-2021 | — | terminated | Evidence of face masks or other material in the seal in several kits, causing improper seals and compromised sterility |