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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
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 1000123297
- DUNS Number
- —
Catalogue (390)
Page 8 of 8| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Trinity Sterile, Inc. | 5023 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 9200 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 7094 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 5068 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 50320 | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | 20202 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 7007 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 5094 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 20319 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 5001 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 50194 | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | T97-772 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 81655 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | T98-386 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | T97-853 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 70552 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 7034 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 85286UCMC2 | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | 81345 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 50910 | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | 50612 | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | 10038 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 50840 | FDA UDI | Class II | Active |
| Trinity Sterile, Inc. | 85376 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 11212 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 20666 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 5020 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | T97-777 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | T98-480 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 85357 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | T98-103 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 6011 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 7005 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 11214 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 81666 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 5052 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 6000 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 81249 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | T97-778 | FDA UDI | Class I | Active |
| Trinity Sterile, Inc. | 6091 | FDA UDI | Class I | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
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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 |